Compositions and Methods for Inhibiting Expression of the PCSK9 Gene

ABSTRACT

The invention relates to a double-stranded ribonucleic acid (dsRNA) for inhibiting the expression of the PCSK9 gene (PCSK9 gene), comprising an antisense strand having a nucleotide sequence which is less that 30 nucleotides in length, generally 19-25 nucleotides in length, and which is substantially complementary to at least a part of the PCSK9 gene. The invention also relates to a pharmaceutical composition comprising the dsRNA together with a pharmaceutically acceptable carrier and method for treating diseases caused by PCSK9 gene expression.

CROSS-REFERENCE TO RELATED APPLICATIONS

This application is a continuation of U.S. application Ser. No.15/807,275, filed Nov. 8, 2017, allowed, which is a continuation of U.S.application Ser. No. 15/005,933, filed Jan. 25, 2016, now U.S. Pat. No.9,822,365, issued Nov. 21, 2017, which is a continuation of U.S.application Ser. No. 14/330,923 filed Jul. 14, 2014, now U.S. Pat. No.9,260,718, issued Feb. 16, 2016, which is a continuation of U.S.application Ser. No. 13/472,438, filed May 15, 2012, now U.S. Pat. No.8,809,292 issued Aug. 19, 2014, which is a continuation of U.S.application Ser. No. 12/554,231, filed Sep. 4, 2009, now U.S. Pat. No.8,222,222, issued on Jul. 17, 2012, which is a divisional of U.S.application Ser. No. 11/746,864, filed May 10, 2007, now U.S. Pat. No.7,605,251, issued on Oct. 20, 2009, which claims the benefit of andpriority to U.S. Provisional Application No. 60/799,458, filed May 11,2006; U.S. Provisional Application No. 60/817,203, filed Jun. 27, 2006;U.S. Provisional Application No. 60/840,089, filed Aug. 25, 2006; U.S.Provisional Application No. 60/829,914, filed Oct. 18, 2006; and U.S.Provisional Application No. 60/901,134, filed Feb. 13, 2007. Thecontents of all of these applications are hereby incorporated byreference in their entirety.

SEQUENCE LISTING

The instant application contains a Sequence Listing which has beensubmitted via EFS-Web and is hereby incorporated by reference in itsentirety. Said ASCII copy, created on Oct. 15, 2019, is namedAYN033C5_sequencelisting.txt, includes 1505 sequences and is 563 KB insize.

FIELD OF THE INVENTION

This invention relates to double-stranded ribonucleic acid (dsRNA), andits use in mediating RNA interference to inhibit the expression of thePCSK9 gene and the use of the dsRNA to treat pathological processeswhich can be mediated by down regulating PCSK9, such as hyperlipidemia.

BACKGROUND OF THE INVENTION

Proprotein convertase subtilisin kexin 9 (PCSK9) is a member of thesubtilisin serine protease family. The other eight mammalian subtilisinproteases, PCSK1-PCSK8 (also called PC1/3, PC2, furin, PC4, PC5/6,PACE4, PC7, and S1P/SKI-1) are proprotein convertases that process awide variety of proteins in the secretory pathway and play roles indiverse biological processes (Bergeron, F. (2000) J. Mol. Endocrinol.24, 1-22, Gensberg, K., (1998) Semin. Cell Dev. Biol. 9, 11-17, Seidah,N. G. (1999) Brain Res. 848, 45-62, Taylor, N. A., (2003) FASEB J. 17,1215-1227, and Zhou, A., (1999) J. Biol. Chem. 274, 20745-20748). PCSK9has been proposed to play a role in cholesterol metabolism. PCSK9 mRNAexpression is down-regulated by dietary cholesterol feeding in mice(Maxwell, K. N., (2003) J. Lipid Res. 44, 2109-2119), up-regulated bystatins in HepG2 cells (Dubuc, G., (2004) Arterioscler. Thromb. Vasc.Biol. 24, 1454-1459), and up-regulated in sterol regulatory elementbinding protein (SREBP) transgenic mice (Horton, J. D., (2003) Proc.Natl. Acad. Sci. USA 100, 12027-12032), similar to the cholesterolbiosynthetic enzymes and the low-density lipoprotein receptor (LDLR).Furthermore, PCSK9 missense mutations have been found to be associatedwith a form of autosomal dominant hypercholesterolemia (Hchola3)(Abifadel, M., et al. (2003) Nat. Genet. 34, 154-156, Timms, K. M.,(2004) Hum. Genet. 114, 349-353, Leren, T. P. (2004) Clin. Genet. 65,419-422). PCSK9 may also play a role in determining LDL cholesterollevels in the general population, because single-nucleotidepolymorphisms (SNPs) have been associated with cholesterol levels in aJapanese population (Shioji, K., (2004) J. Hum. Genet. 49, 109-114).

Autosomal dominant hypercholesterolemias (ADHs) are monogenic diseasesin which patients exhibit elevated total and LDL cholesterol levels,tendon xanthomas, and premature atherosclerosis (Rader, D. J., (2003) J.Clin. Invest. 111, 1795-1803). The pathogenesis of ADHs and a recessiveform, autosomal recessive hypercholesterolemia (ARH) (Cohen, J. C.,(2003) Curr. Opin. Lipidol. 14, 121-127), is due to defects in LDLuptake by the liver. ADH may be caused by LDLR mutations, which preventLDL uptake, or by mutations in the protein on LDL, apolipoprotein B,which binds to the LDLR. ARH is caused by mutations in the ARH proteinthat are necessary for endocytosis of the LDLR-LDL complex via itsinteraction with clathrin. Therefore, if PCSK9 mutations are causativein Hchola3 families, it seems likely that PCSK9 plays a role inreceptor-mediated LDL uptake.

Overexpression studies point to a role for PCSK9 in controlling LDLRlevels and, hence, LDL uptake by the liver (Maxwell, K. N. (2004) Proc.Natl. Acad. Sci. USA 101, 7100-7105, Benjannet, S., et al. (2004) J.Biol. Chem. 279, 48865-48875, Park, S. W., (2004) J. Biol. Chem. 279,50630-50638). Adenoviral-mediated overexpression of mouse or human PCSK9for 3 or 4 days in mice results in elevated total and LDL cholesterollevels; this effect is not seen in LDLR knockout animals (Maxwell, K. N.(2004) Proc. Natl. Acad. Sci. USA 101, 7100-7105, Benjannet, S., et al.(2004) J. Biol. Chem. 279, 48865-48875, Park, S. W., (2004) J. Biol.Chem. 279, 50630-50638). In addition, PCSK9 overexpression results in asevere reduction in hepatic LDLR protein, without affecting LDLR mRNAlevels, SREBP protein levels, or SREBP protein nuclear to cytoplasmicratio. These results indicate that PCSK9, either directly or indirectly,reduces LDLR protein levels by a posttranscriptional mechanism

Loss of function mutations in PCSK9 have been designed in mouse models(Rashid et. al., (2005) PNAS, 102, 5374-5379., and identified in humanindividuals Cohen et al., (2005), Nature Genetics., 37, 161-165. In bothcases loss of PCSK9 function lead to lowering of total and LDLccholesterol. In a retrospective outcome study over 15 years, loss of onecopy of PCSK9 was shown to shift LDLc lower and to lead to an increasedrisk-benefit protection from developing cardiovascular heart disease(Cohen et.al., 2006 N. Engl. J. Med., 354., 1264-1272.). Clearly theevidence to date indicates that lowering of PCSK9 levels will lowerLDLc.

Recently, double-stranded RNA molecules (dsRNA) have been shown to blockgene expression in a highly conserved regulatory mechanism known as RNAinterference (RNAi). WO 99/32619 (Fire et al.) discloses the use of adsRNA of at least 25 nucleotides in length to inhibit the expression ofgenes in C. elegans. dsRNA has also been shown to degrade target RNA inother organisms, including plants (see, e.g., WO 99/53050, Waterhouse etal.; and WO 99/61631, Heifetz et al.), Drosophila (see, e.g., Yang, D.,et al., Curr. Biol. (2000) 10:1191-1200), and mammals (see WO 00/44895,Limmer; and DE 101 00 586.5, Kreutzer et al.). This natural mechanismhas now become the focus for the development of a new class ofpharmaceutical agents for treating disorders that are caused by theaberrant or unwanted regulation of a gene.

Despite significant advances in the field of RNAi and advances in thetreatment of pathological processes which can be mediated by downregulating PCSK9 gene expression, there remains a need for agents thatcan inhibit PCSK9 gene expression and that can treat diseases associatedwith PCSK9 gene expression such as hyperlipidemia.

SUMMARY OF THE INVENTION

The invention provides a solution to the problem of treating diseasesthat can be modulated by down regulating the proprotein convertasesubtilisin kexin 9 (PCSK9) by using double-stranded ribonucleic acid(dsRNA) to silence PCSK9 expression.

The invention provides double-stranded ribonucleic acid (dsRNA), as wellas compositions and methods for inhibiting the expression of the PCSK9gene in a cell or mammal using such dsRNA. The invention also providescompositions and methods for treating pathological conditions that canmodulated by down regulating the expression of the PCSK9 gene, such ashyperlipidemia. The dsRNA of the invention comprises an RNA strand (theantisense strand) having a region which is less than 30 nucleotides inlength, generally 19-24 nucleotides in length, and is substantiallycomplementary to at least part of an mRNA transcript of the PCSK9 gene.

In one embodiment, the invention provides double-stranded ribonucleicacid (dsRNA) molecules for inhibiting the expression of the PCSK9 gene.The dsRNA comprises at least two sequences that are complementary toeach other. The dsRNA comprises a sense strand comprising a firstsequence and an antisense strand comprising a second sequence. Theantisense strand comprises a nucleotide sequence which is substantiallycomplementary to at least part of an mRNA encoding PCSK9, and the regionof complementarity is less than 30 nucleotides in length, generally19-24 nucleotides in length. The dsRNA, upon contacting with a cellexpressing the PCSK9, inhibits the expression of the PCSK9 gene by atleast 40%.

For example, the dsRNA molecules of the invention can be comprised of afirst sequence of the dsRNA that is selected from the group consistingof the sense sequences of Table 1 and Table 2 the second sequence isselected from the group consisting of the antisense sequences of Tables1 and Table 2. The dsRNA molecules of the invention can be comprised ofnaturally occurring nucleotides or can be comprised of at least onemodified nucleotide, such as a 2′-O-methyl modified nucleotide, anucleotide comprising a 5′-phosphorothioate group, and a terminalnucleotide linked to a cholesteryl derivative. Alternatively, themodified nucleotide may be chosen from the group of: a2′-deoxy-2′-fluoro modified nucleotide, a 2′-deoxy-modified nucleotide,a locked nucleotide, an abasic nucleotide, 2′-amino-modified nucleotide,2′-alkyl-modified nucleotide, morpholino nucleotide, a phosphoramidate,and a non-natural base comprising nucleotide. Generally, such modifiedsequence will be based on a first sequence of the dsRNA selected fromthe group consisting of the sense sequences of Tables 1 and Table 2 anda second sequence selected from the group consisting of the antisensesequences of Tables 1, and Table 2.

In another embodiment, the invention provides a cell comprising one ofthe dsRNAs of the invention. The cell is generally a mammalian cell,such as a human cell.

In another embodiment, the invention provides a pharmaceuticalcomposition for inhibiting the expression of the PCSK9 gene in anorganism, generally a human subject, comprising one or more of the dsRNAof the invention and a pharmaceutically acceptable carrier or deliveryvehicle.

In another embodiment, the invention provides a method for inhibitingthe expression of the PCSK9 gene in a cell, comprising the followingsteps:

-   -   (a) introducing into the cell a double-stranded ribonucleic acid        (dsRNA), wherein the dsRNA comprises at least two sequences that        are complementary to each other. The dsRNA comprises a sense        strand comprising a first sequence and an antisense strand        comprising a second sequence. The antisense strand comprises a        region of complementarity which is substantially complementary        to at least a part of a mRNA encoding PCSK9, and wherein the        region of complementarity is less than 30 nucleotides in length,        generally 19-24 nucleotides in length, and wherein the dsRNA,        upon contact with a cell expressing the PCSK9, inhibits        expression of the PCSK9 gene by at least 40%; and    -   (b) maintaining the cell produced in step (a) for a time        sufficient to obtain degradation of the mRNA transcript of the        PCSK9 gene, thereby inhibiting expression of the PCSK9 gene in        the cell.

In another embodiment, the invention provides methods for treating,preventing or managing pathological processes which can be mediated bydown regulating PCSK9 gene expression, e.g. hyperlipidemia, comprisingadministering to a patient in need of such treatment, prevention ormanagement a therapeutically or prophylactically effective amount of oneor more of the dsRNAs of the invention.

In another embodiment, the invention provides vectors for inhibiting theexpression of the PCSK9 gene in a cell, comprising a regulatory sequenceoperably linked to a nucleotide sequence that encodes at least onestrand of one of the dsRNA of the invention.

In another embodiment, the invention provides a cell comprising a vectorfor inhibiting the expression of the PCSK9 gene in a cell. The vectorcomprises a regulatory sequence operably linked to a nucleotide sequencethat encodes at least one strand of one of the dsRNA of the invention.

BRIEF DESCRIPTION OF THE FIGURES

FIG. 1 shows the structure of the ND-98 lipid.

FIG. 2 shows the results of the in vivo screen of 16 mouse specific(AL-DP-9327 through AL-DP-9342) PCSK9 siRNAs directed against differentORF regions of PCSK9 mRNA (having the first nucleotide corresponding tothe ORF position indicated on the graph) in C57/BL6 mice (5animals/group). The ratio of PCSK9 mRNA to GAPDH mRNA in liver lysateswas averaged over each treatment group and compared to a control grouptreated with PBS or a control group treated with an unrelated siRNA(blood coagulation factor VII).

FIG. 3 shows the results of the in vivo screen of 16 human/mouse/ratcrossreactive (AL-DP-9311 through AL-DP-9326) PCSK9 siRNAs directedagainst different ORF regions of PCSK9 mRNA (having the first nucleotidecorresponding to the ORF position indicated on the graph) in C57/BL6mice (5 animals/group). The ratio of PCSK9 mRNA to GAPDH mRNA in liverlysates was averaged over each treatment group and compared to a controlgroup treated with PBS or a control group treated with an unrelatedsiRNA (blood coagulation factor VII). Silencing of PCSK9 mRNA resultedin lowering total serum cholesterol levels. The most efficacious interms of knocking down PSCK9 message siRNAs showed the most pronouncedcholesterol lowering effect (around 20-30%).

FIG. 4 shows the results of the in vivo screen of 16 mouse specific(AL-DP-9327 through AL-DP-9342) PCSK9 siRNAs in C57/BL6 mice (5animals/group). Total serum cholesterol levels were averaged over eachtreatment group and compared to a control group treated with PBS or acontrol group treated with an unrelated siRNA (blood coagulation factorVII).

FIG. 5 shows the results of the in vivo screen of 16 human/mouse/ratcrossreactive (AL-DP-9311 through AL-DP-9326) PCSK9 siRNAs in C57/BL6mice (5 animals/group). Total serum cholesterol levels were averagedover each treatment group and compared to a control group treated withPBS or a control group treated with an unrelated siRNA (bloodcoagulation factor VII).

FIG. 6A and FIG. 6B each shows a comparison of the in vitro and in vivoresults for silencing PCSK9.

FIG. 7A and FIG. 7B show in vitro results for silencing PCSK9 usingmonkey primary hepatocytes.

FIG. 8 shows in vivo activity of LNP-01 formulated siRNAs to pcsk-9.

FIG. 9 shows in vivo activity of LNP-01 Formulated chemically modified9314 and 10792 parent molecules at different times. Clearly modifiedversions of 10792 display in vivo silencing activity.

DETAILED DESCRIPTION OF THE INVENTION

The invention provides a solution to the problem of treating diseasesthat can be modulated by the down regulation of the PCSK9 gene, by usingdouble-stranded ribonucleic acid (dsRNA) to silence the PCSK9 gene thusproviding treatment for diseases such as hyperlipidemia.

The invention provides double-stranded ribonucleic acid (dsRNA), as wellas compositions and methods for inhibiting the expression of the PCSK9gene in a cell or mammal using the dsRNA. The invention also providescompositions and methods for treating pathological conditions anddiseases that can be modulated by down regulating the expression of thePCSK9 gene. dsRNA directs the sequence-specific degradation of mRNAthrough a process known as RNA interference (RNAi).

The dsRNA of the invention comprises an RNA strand (the antisensestrand) having a region which is less than 30 nucleotides in length,generally 19-24 nucleotides in length, and is substantiallycomplementary to at least part of an mRNA transcript of the PCSK9 gene.The use of these dsRNAs enables the targeted degradation of an mRNA thatis involved in sodium transport. Using cell-based and animal assays, thepresent inventors have demonstrated that very low dosages of these dsRNAcan specifically and efficiently mediate RNAi, resulting in significantinhibition of expression of the PCSK9 gene. Thus, the methods andcompositions of the invention comprising these dsRNAs are useful fortreating pathological processes which can be mediated by down regulatingPCSK9, such as in the treatment of hyperlipidemia.

The following detailed description discloses how to make and use thedsRNA and compositions containing dsRNA to inhibit the expression of thetarget PCSK9 gene, as well as compositions and methods for treatingdiseases that can be modulated by down regulating the expression ofPCSK9, such as hyperlipidemia. The pharmaceutical compositions of theinvention comprise a dsRNA having an antisense strand comprising aregion of complementarity which is less than 30 nucleotides in length,generally 19-24 nucleotides in length, and is substantiallycomplementary to at least part of an RNA transcript of the PCSK9 gene,together with a pharmaceutically acceptable carrier.

Accordingly, certain aspects of the invention provide pharmaceuticalcompositions comprising the dsRNA of the invention together with apharmaceutically acceptable carrier, methods of using the compositionsto inhibit expression of the PCSK9 gene, and methods of using thepharmaceutical compositions to treat diseases that can be modulated bydown regulating the expression of PCSK9.

I. Definitions

For convenience, the meaning of certain terms and phrases used in thespecification, examples, and appended claims, are provided below. Ifthere is an apparent discrepancy between the usage of a term in otherparts of this specification and its definition provided in this section,the definition in this section shall prevail.

“G,” “C,” “A” and “U” each generally stand for a nucleotide thatcontains guanine, cytosine, adenine, and uracil as a base, respectively.However, it will be understood that the term “ribonucleotide” or“nucleotide” can also refer to a modified nucleotide, as furtherdetailed below, or a surrogate replacement moiety. The skilled person iswell aware that guanine, cytosine, adenine, and uracil may be replacedby other moieties without substantially altering the base pairingproperties of an oligonucleotide comprising a nucleotide bearing suchreplacement moiety. For example, without limitation, a nucleotidecomprising inosine as its base may base pair with nucleotides containingadenine, cytosine, or uracil. Hence, nucleotides containing uracil,guanine, or adenine may be replaced in the nucleotide sequences of theinvention by a nucleotide containing, for example, inosine. Sequencescomprising such replacement moieties are embodiments of the invention.

As used herein, “PCSK9” refers to the proprotein convertase subtilisinkexin 9 gene or protein (also known as FH3, HCHOLA3, NARC-1, NARC1).mRNA sequences to PCSK9 are provided as human: NM_174936; mouse:NM_153565, and rat: NM_199253.

As used herein, “target sequence” refers to a contiguous portion of thenucleotide sequence of an mRNA molecule formed during the transcriptionof the PCSK9 gene, including mRNA that is a product of RNA processing ofa primary transcription product.

As used herein, the term “strand comprising a sequence” refers to anoligonucleotide comprising a chain of nucleotides that is described bythe sequence referred to using the standard nucleotide nomenclature.

As used herein, and unless otherwise indicated, the term“complementary,” when used to describe a first nucleotide sequence inrelation to a second nucleotide sequence, refers to the ability of anoligonucleotide or polynucleotide comprising the first nucleotidesequence to hybridize and form a duplex structure under certainconditions with an oligonucleotide or polynucleotide comprising thesecond nucleotide sequence, as will be understood by the skilled person.Such conditions can, for example, be stringent conditions, wherestringent conditions may include: 400 mM NaCl, 40 mM PIPES pH 6.4, 1 mMEDTA, 50° C. or 70° C. for 12-16 hours followed by washing. Otherconditions, such as physiologically relevant conditions as may beencountered inside an organism, can apply. The skilled person will beable to determine the set of conditions most appropriate for a test ofcomplementarity of two sequences in accordance with the ultimateapplication of the hybridized nucleotides.

This includes base-pairing of the oligonucleotide or polynucleotidecomprising the first nucleotide sequence to the oligonucleotide orpolynucleotide comprising the second nucleotide sequence over the entirelength of the first and second nucleotide sequence. Such sequences canbe referred to as “fully complementary” with respect to each otherherein. However, where a first sequence is referred to as “substantiallycomplementary” with respect to a second sequence herein, the twosequences can be fully complementary, or they may form one or more, butgenerally not more than 4, 3 or 2 mismatched base pairs uponhybridization, while retaining the ability to hybridize under theconditions most relevant to their ultimate application. However, wheretwo oligonucleotides are designed to form, upon hybridization, one ormore single stranded overhangs, such overhangs shall not be regarded asmismatches with regard to the determination of complementarity. Forexample, a dsRNA comprising one oligonucleotide 21 nucleotides in lengthand another oligonucleotide 23 nucleotides in length, wherein the longeroligonucleotide comprises a sequence of 21 nucleotides that is fullycomplementary to the shorter oligonucleotide, may yet be referred to as“fully complementary” for the purposes of the invention.

“Complementary” sequences, as used herein, may also include, or beformed entirely from, non-Watson-Crick base pairs and/or base pairsformed from non-natural and modified nucleotides, in as far as the aboverequirements with respect to their ability to hybridize are fulfilled.

The terms “complementary”, “fully complementary” and “substantiallycomplementary” herein may be used with respect to the base matchingbetween the sense strand and the antisense strand of a dsRNA, or betweenthe antisense strand of a dsRNA and a target sequence, as will beunderstood from the context of their use.

As used herein, a polynucleotide which is “substantially complementaryto at least part of” a messenger RNA (mRNA) refers to a polynucleotidewhich is substantially complementary to a contiguous portion of the mRNAof interest (e.g., encoding PCSK9). For example, a polynucleotide iscomplementary to at least a part of a PCSK9 mRNA if the sequence issubstantially complementary to a non-interrupted portion of a mRNAencoding PCSK9.

The term “double-stranded RNA” or “dsRNA”, as used herein, refers to acomplex of ribonucleic acid molecules, having a duplex structurecomprising two anti-parallel and substantially complementary, as definedabove, nucleic acid strands. The two strands forming the duplexstructure may be different portions of one larger RNA molecule, or theymay be separate RNA molecules. Where separate RNA molecules, such dsRNAare often referred to in the literature as siRNA (“short interferingRNA”). Where the two strands are part of one larger molecule, andtherefore are connected by an uninterrupted chain of nucleotides betweenthe 3′-end of one strand and the 5′ end of the respective other strandforming the duplex structure, the connecting RNA chain is referred to asa “hairpin loop”, “short hairpin RNA” or “shRNA”. Where the two strandsare connected covalently by means other than an uninterrupted chain ofnucleotides between the 3′-end of one strand and the 5′ end of therespective other strand forming the duplex structure, the connectingstructure is referred to as a “linker”. The RNA strands may have thesame or a different number of nucleotides. The maximum number of basepairs is the number of nucleotides in the shortest strand of the dsRNAminus any overhangs that are present in the duplex. In addition to theduplex structure, a dsRNA may comprise one or more nucleotide overhangs.In addition, as used in this specification, “dsRNA” may include chemicalmodifications to ribonucleotides, including substantial modifications atmultiple nucleotides and including all types of modifications disclosedherein or known in the art. Any such modifications, as used in an siRNAtype molecule, are encompassed by “dsRNA” for the purposes of thisspecification and claims.

As used herein, a “nucleotide overhang” refers to the unpairednucleotide or nucleotides that protrude from the duplex structure of adsRNA when a 3′-end of one strand of the dsRNA extends beyond the 5′-endof the other strand, or vice versa. “Blunt” or “blunt end” means thatthere are no unpaired nucleotides at that end of the dsRNA, i.e., nonucleotide overhang. A “blunt ended” dsRNA is a dsRNA that isdouble-stranded over its entire length, i.e., no nucleotide overhang ateither end of the molecule. For clarity, chemical caps or non-nucleotidechemical moieties conjugated to the 3′ end or 5′ end of an siRNA are notconsidered in determining whether an siRNA has an overhang or is bluntended.

The term “antisense strand” refers to the strand of a dsRNA whichincludes a region that is substantially complementary to a targetsequence. As used herein, the term “region of complementarity” refers tothe region on the antisense strand that is substantially complementaryto a sequence, for example a target sequence, as defined herein. Wherethe region of complementarity is not fully complementary to the targetsequence, the mismatches are most tolerated in the terminal regions and,if present, are generally in a terminal region or regions, e.g., within6, 5, 4, 3, or 2 nucleotides of the 5′ and/or 3′ terminus.

The term “sense strand,” as used herein, refers to the strand of a dsRNAthat includes a region that is substantially complementary to a regionof the antisense strand.

“Introducing into a cell”, when referring to a dsRNA, means facilitatinguptake or absorption into the cell, as is understood by those skilled inthe art. Absorption or uptake of dsRNA can occur through unaideddiffusive or active cellular processes, or by auxiliary agents ordevices. The meaning of this term is not limited to cells in vitro; adsRNA may also be “introduced into a cell”, wherein the cell is part ofa living organism. In such instance, introduction into the cell willinclude the delivery to the organism. For example, for in vivo delivery,dsRNA can be injected into a tissue site or administered systemically.In vitro introduction into a cell includes methods known in the art suchas electroporation and lipofection.

The terms “silence” and “inhibit the expression of”, in as far as theyrefer to the PCSK9 gene, herein refer to the at least partialsuppression of the expression of the PCSK9 gene, as manifested by areduction of the amount of mRNA transcribed from the PCSK9 gene whichmay be isolated from a first cell or group of cells in which the PCSK9gene is transcribed and which has or have been treated such that theexpression of the PCSK9 gene is inhibited, as compared to a second cellor group of cells substantially identical to the first cell or group ofcells but which has or have not been so treated (control cells). Thedegree of inhibition is usually expressed in terms of

(mRNA in control cells)−(mRNA in treated cells)/(mRNA in controlcells)·100%

Alternatively, the degree of inhibition may be given in terms of areduction of a parameter that is functionally linked to PCSK9 genetranscription, e.g. the amount of protein encoded by the PCSK9 genewhich is secreted by a cell, or the number of cells displaying a certainphenotype, e.g apoptosis. In principle, PCSK9 gene silencing may bedetermined in any cell expressing the target, either constitutively orby genomic engineering, and by any appropriate assay. However, when areference is needed in order to determine whether a given dsRNA inhibitsthe expression of the PCSK9 gene by a certain degree and therefore isencompassed by the instant invention, the assay provided in the Examplesbelow shall serve as such reference.

For example, in certain instances, expression of the PCSK9 gene issuppressed by at least about 20%, 25%, 35%, or 50% by administration ofthe double-stranded oligonucleotide of the invention. In someembodiment, the PCSK9 gene is suppressed by at least about 60%, 70%, or80% by administration of the double-stranded oligonucleotide of theinvention. In some embodiments, the PCSK9 gene is suppressed by at leastabout 85%, 90%, or 95% by administration of the double-strandedoligonucleotide of the invention. Tables 1, 2, provides a wide range ofvalues for inhibition of expression obtained in an in vitro assay usingvarious PCSK9 dsRNA molecules at various concentrations.

As used herein in the context of PCSK9 expression, the terms “treat”,“treatment”, and the like, refer to relief from or alleviation ofpathological processes which can be mediated by down regulating PCSK9gene. In the context of the present invention insofar as it relates toany of the other conditions recited herein below (other thanpathological processes which can be mediated by down regulating thePCSK9 gene), the terms “treat”, “treatment”, and the like mean torelieve or alleviate at least one symptom associated with suchcondition, or to slow or reverse the progression of such condition. Forexample, in the context of hyperlipidemia, treatment will involve adecrease in serum lipid levels.

As used herein, the phrases “therapeutically effective amount” and“prophylactically effective amount” refer to an amount that provides atherapeutic benefit in the treatment, prevention, or management ofpathological processes which can be mediated by down regulating thePCSK9 gene on or an overt symptom of pathological processes which can bemediated by down regulating the PCSK9 gene. The specific amount that istherapeutically effective can be readily determined by ordinary medicalpractitioner, and may vary depending on factors known in the art, suchas, e.g. the type of pathological processes which can be mediated bydown regulating the PCSK9 gene, the patient's history and age, the stageof pathological processes which can be mediated by down regulating PCSK9gene expression, and the administration of other anti-pathologicalprocesses which can be mediated by down regulating PCSK9 geneexpression.

As used herein, a “pharmaceutical composition” comprises apharmacologically effective amount of a dsRNA and a pharmaceuticallyacceptable carrier. As used herein, “pharmacologically effectiveamount,” “therapeutically effective amount” or simply “effective amount”refers to that amount of an RNA effective to produce the intendedpharmacological, therapeutic or preventive result. For example, if agiven clinical treatment is considered effective when there is at leasta 25% reduction in a measurable parameter associated with a disease ordisorder, a therapeutically effective amount of a drug for the treatmentof that disease or disorder is the amount necessary to effect at least a25% reduction in that parameter.

The term “pharmaceutically acceptable carrier” refers to a carrier foradministration of a therapeutic agent. Such carriers include, but arenot limited to, saline, buffered saline, dextrose, water, glycerol,ethanol, and combinations thereof and are described in more detailbelow. The term specifically excludes cell culture medium.

As used herein, a “transformed cell” is a cell into which a vector hasbeen introduced from which a dsRNA molecule may be expressed.

II. Double-Stranded Ribonucleic Acid (dsRNA)

In one embodiment, the invention provides double-stranded ribonucleicacid (dsRNA) molecules for inhibiting the expression of the PCSK9 genein a cell or mammal, wherein the dsRNA comprises an antisense strandcomprising a region of complementarity which is complementary to atleast a part of an mRNA formed in the expression of the PCSK9 gene, andwherein the region of complementarity is less than 30 nucleotides inlength, generally 19-24 nucleotides in length, and wherein the dsRNA,upon contact with a cell expressing the PCSK9 gene, inhibits theexpression of the PCSK9 gene by at least 40%. The dsRNA comprises twoRNA strands that are sufficiently complementary to hybridize to form aduplex structure. One strand of the dsRNA (the antisense strand)comprises a region of complementarity that is substantiallycomplementary, and generally fully complementary, to a target sequence,derived from the sequence of an mRNA formed during the expression of thePCSK9 gene, the other strand (the sense strand) comprises a region whichis complementary to the antisense strand, such that the two strandshybridize and form a duplex structure when combined under suitableconditions. Generally, the duplex structure is between 15 and 30, moregenerally between 18 and 25, yet more generally between 19 and 24, andmost generally between 19 and 21 base pairs in length. Similarly, theregion of complementarity to the target sequence is between 15 and 30,more generally between 18 and 25, yet more generally between 19 and 24,and most generally between 19 and 21 nucleotides in length. The dsRNA ofthe invention may further comprise one or more single-strandednucleotide overhang(s). The dsRNA can be synthesized by standard methodsknown in the art as further discussed below, e.g., by use of anautomated DNA synthesizer, such as are commercially available from, forexample, Biosearch, Applied Biosystems, Inc. In a preferred embodiment,the PCSK9 gene is the human PCSK9 gene. In specific embodiments, theantisense strand of the dsRNA comprises a strand selected from the sensesequences of Tables 1 and 2, and a second sequence selected from thegroup consisting of the antisense sequences of Tables 1 and 2.Alternative antisense agents that target elsewhere in the targetsequence provided in Tables 1 and 2, can readily be determined using thetarget sequence and the flanking PCSK9 sequence.

In further embodiments, the dsRNA comprises at least one nucleotidesequence selected from the groups of sequences provided in Tables 1 and2. In other embodiments, the dsRNA comprises at least two sequencesselected from this group, wherein one of the at least two sequences iscomplementary to another of the at least two sequences, and one of theat least two sequences is substantially complementary to a sequence ofan mRNA generated in the expression of the PCSK9 gene. Generally, thedsRNA comprises two oligonucleotides, wherein one oligonucleotide isdescribed as the sense strand in Tables 1 and 2 and the secondoligonucleotide is described as the antisense strand in Tables 1 and 2

The skilled person is well aware that dsRNAs comprising a duplexstructure of between 20 and 23, but specifically 21, base pairs havebeen hailed as particularly effective in inducing RNA interference(Elbashir et al., EMBO 2001, 20:6877-6888). However, others have foundthat shorter or longer dsRNAs can be effective as well. In theembodiments described above, by virtue of the nature of theoligonucleotide sequences provided in Tables 1 and 2, the dsRNAs of theinvention can comprise at least one strand of a length of minimally 21nt. It can be reasonably expected that shorter dsRNAs comprising one ofthe sequences of Tables 1 and 2 minus only a few nucleotides on one orboth ends may be similarly effective as compared to the dsRNAs describedabove. Hence, dsRNAs comprising a partial sequence of at least 15, 16,17, 18, 19, 20, or more contiguous nucleotides from one of the sequencesof Tables 1 and 2, and differing in their ability to inhibit theexpression of the PCSK9 gene in a FACS assay as described herein belowby not more than 5, 10, 15, 20, 25, or 30% inhibition from a dsRNAcomprising the full sequence, are contemplated by the invention. FurtherdsRNAs that cleave within the target sequence provided in Tables 1 and 2can readily be made using the PCSK9 sequence and the target sequenceprovided.

In addition, the RNAi agents provided in Tables 1 and 2 identify a sitein the PCSK9 mRNA that is susceptible to RNAi based cleavage. As suchthe present invention further includes RNAi agents that target withinthe sequence targeted by one of the agents of the present invention. Asused herein a second RNAi agent is the to target within the sequence ofa first RNAi agent if the second RNAi agent cleaves the message anywherewithin the mRNA that is complementary to the antisense strand of thefirst RNAi agent. Such a second agent will generally consist of at least15 contiguous nucleotides from one of the sequences provided in Tables 1and 2 coupled to additional nucleotide sequences taken from the regioncontiguous to the selected sequence in the PCSK9 gene. For example, thelast 15 nucleotides of SEQ ID NO:1 (minus the added AA sequences)combined with the next 6 nucleotides from the target PCSK9 gene producesa single strand agent of 21 nucleotides that is based on one of thesequences provided in Tables 1 and 2.

The dsRNA of the invention can contain one or more mismatches to thetarget sequence. In a preferred embodiment, the dsRNA of the inventioncontains no more than 3 mismatches. If the antisense strand of the dsRNAcontains mismatches to a target sequence, it is preferable that the areaof mismatch not be located in the center of the region ofcomplementarity. If the antisense strand of the dsRNA containsmismatches to the target sequence, it is preferable that the mismatch berestricted to 5 nucleotides from either end, for example 5, 4, 3, 2, or1 nucleotide from either the 5′ or 3′ end of the region ofcomplementarity. For example, for a 23 nucleotide dsRNA strand which iscomplementary to a region of the PCSK9 gene, the dsRNA generally doesnot contain any mismatch within the central 13 nucleotides. The methodsdescribed within the invention can be used to determine whether a dsRNAcontaining a mismatch to a target sequence is effective in inhibitingthe expression of the PCSK9 gene. Consideration of the efficacy ofdsRNAs with mismatches in inhibiting expression of the PCSK9 gene isimportant, especially if the particular region of complementarity in thePCSK9 gene is known to have polymorphic sequence variation within thepopulation.

In one embodiment, at least one end of the dsRNA has a single-strandednucleotide overhang of 1 to 4, generally 1 or 2 nucleotides. dsRNAshaving at least one nucleotide overhang have unexpectedly superiorinhibitory properties than their blunt-ended counterparts. Moreover, thepresent inventors have discovered that the presence of only onenucleotide overhang strengthens the interference activity of the dsRNA,without affecting its overall stability. dsRNA having only one overhanghas proven particularly stable and effective in vivo, as well as in avariety of cells, cell culture mediums, blood, and serum. Generally, thesingle-stranded overhang is located at the 3′-terminal end of theantisense strand or, alternatively, at the 3′-terminal end of the sensestrand. The dsRNA may also have a blunt end, generally located at the5′-end of the antisense strand. Such dsRNAs have improved stability andinhibitory activity, thus allowing administration at low dosages, i.e.,less than 5 mg/kg body weight of the recipient per day. Generally, theantisense strand of the dsRNA has a nucleotide overhang at the 3′-end,and the 5′-end is blunt. In another embodiment, one or more of thenucleotides in the overhang is replaced with a nucleoside thiophosphate.

In yet another embodiment, the dsRNA is chemically modified to enhancestability. The nucleic acids of the invention may be synthesized and/ormodified by methods well established in the art, such as those describedin “Current protocols in nucleic acid chemistry”, Beaucage, S. L. et al.(Edrs.), John Wiley & Sons, Inc., New York, N.Y., USA, which is herebyincorporated herein by reference. Chemical modifications may include,but are not limited to 2′ modifications, modifications at other sites ofthe sugar or base of an oligonucleotide, introduction of non-naturalbases into the olibonucleotide chain, covalent attachment to a ligand orchemical moiety, and replacement of internucleotide phosphate linkageswith alternate linkages such as thiophosphates. More than one suchmodification may be employed.

Chemical linking of the two separate dsRNA strands may be achieved byany of a variety of well-known techniques, for example by introducingcovalent, ionic or hydrogen bonds; hydrophobic interactions, van derWaals or stacking interactions; by means of metal-ion coordination, orthrough use of purine analogues. Generally, the chemical groups that canbe used to modify the dsRNA include, without limitation, methylene blue;bifunctional groups, generally bis-(2-chloroethyl)amine;N-acetyl-N′-(p-glyoxylbenzoyl)cystamine; 4-thiouracil; and psoralen. Inone embodiment, the linker is a hexa-ethylene glycol linker. In thiscase, the dsRNA are produced by solid phase synthesis and thehexa-ethylene glycol linker is incorporated according to standardmethods (e.g., Williams, D. J., and K. B. Hall, Biochem. (1996)35:14665-14670). In a particular embodiment, the 5′-end of the antisensestrand and the 3′-end of the sense strand are chemically linked via ahexaethylene glycol linker. In another embodiment, at least onenucleotide of the dsRNA comprises a phosphorothioate orphosphorodithioate groups. The chemical bond at the ends of the dsRNA isgenerally formed by triple-helix bonds. Tables 1 and 2 provides examplesof modified RNAi agents of the invention.

In yet another embodiment, the nucleotides at one or both of the twosingle strands may be modified to prevent or inhibit the degradationactivities of cellular enzymes, such as, for example, withoutlimitation, certain nucleases. Techniques for inhibiting the degradationactivity of cellular enzymes against nucleic acids are known in the artincluding, but not limited to, 2′-amino modifications, 2′-amino sugarmodifications, 2′-F sugar modifications, 2′-F modifications, 2′-alkylsugar modifications, uncharged backbone modifications, morpholinomodifications, 2′-O-methyl modifications, and phosphoramidate (see,e.g., Wagner, Nat. Med. (1995) 1:1116-8). Thus, at least one 2′-hydroxylgroup of the nucleotides on a dsRNA is replaced by a chemical group,generally by a 2′-amino or a 2′-methyl group. Also, at least onenucleotide may be modified to form a locked nucleotide. Such lockednucleotide contains a methylene bridge that connects the 2′-oxygen ofribose with the 4′-carbon of ribose. Oligonucleotides containing thelocked nucleotide are described in Koshkin, A. A., et al., Tetrahedron(1998), 54: 3607-3630) and Obika, S. et al., Tetrahedron Lett. (1998),39: 5401-5404). Introduction of a locked nucleotide into anoligonucleotide improves the affinity for complementary sequences andincreases the melting temperature by several degrees (Braasch, D. A. andD. R. Corey, Chem. Biol. (2001), 8:1-7).

Conjugating a ligand to a dsRNA can enhance its cellular absorption aswell as targeting to a particular tissue or uptake by specific types ofcells such as liver cells. In certain instances, a hydrophobic ligand isconjugated to the dsRNA to facilitate direct permeation of the cellularmembrane and or uptake across the liver cells. Alternatively, the ligandconjugated to the dsRNA is a substrate for receptor-mediatedendocytosis. These approaches have been used to facilitate cellpermeation of antisense oligonucleotides as well as dsRNA agents. Forexample, cholesterol has been conjugated to various antisenseoligonucleotides resulting in compounds that are substantially moreactive compared to their non-conjugated analogs. See M. ManoharanAntisense & Nucleic Acid Drug Development 2002, 12, 103. Otherlipophilic compounds that have been conjugated to oligonucleotidesinclude 1-pyrene butyric acid, 1,3-bis-O-(hexadecyl)glycerol, andmenthol. One example of a ligand for receptor-mediated endocytosis isfolic acid. Folic acid enters the cell by folate-receptor-mediatedendocytosis. dsRNA compounds bearing folic acid would be efficientlytransported into the cell via the folate-receptor-mediated endocytosis.Li and coworkers report that attachment of folic acid to the 3′-terminusof an oligonucleotide resulted in an 8-fold increase in cellular uptakeof the oligonucleotide. Li, S.; Deshmukh, H. M.; Huang, L. Pharm. Res.1998, 15, 1540. Other ligands that have been conjugated tooligonucleotides include polyethylene glycols, carbohydrate clusters,cross-linking agents, porphyrin conjugates, delivery peptides and lipidssuch as cholesterol.

In certain instances, conjugation of a cationic ligand tooligonucleotides results in improved resistance to nucleases.Representative examples of cationic ligands are propylammonium anddimethylpropylammonium. Interestingly, antisense oligonucleotides werereported to retain their high binding affinity to mRNA when the cationicligand was dispersed throughout the oligonucleotide. See M. ManoharanAntisense & Nucleic Acid Drug Development 2002, 12, 103 and referencestherein.

The ligand-conjugated dsRNA of the invention may be synthesized by theuse of a dsRNA that bears a pendant reactive functionality, such as thatderived from the attachment of a linking molecule onto the dsRNA. Thisreactive oligonucleotide may be reacted directly withcommercially-available ligands, ligands that are synthesized bearing anyof a variety of protecting groups, or ligands that have a linking moietyattached thereto. The methods of the invention facilitate the synthesisof ligand-conjugated dsRNA by the use of, in some preferred embodiments,nucleoside monomers that have been appropriately conjugated with ligandsand that may further be attached to a solid-support material. Suchligand-nucleoside conjugates, optionally attached to a solid-supportmaterial, are prepared according to some preferred embodiments of themethods of the invention via reaction of a selected serum-binding ligandwith a linking moiety located on the 5′ position of a nucleoside oroligonucleotide. In certain instances, an dsRNA bearing an aralkylligand attached to the 3′-terminus of the dsRNA is prepared by firstcovalently attaching a monomer building block to a controlled-pore-glasssupport via a long-chain aminoalkyl group. Then, nucleotides are bondedvia standard solid-phase synthesis techniques to the monomerbuilding-block bound to the solid support. The monomer building blockmay be a nucleoside or other organic compound that is compatible withsolid-phase synthesis.

The dsRNA used in the conjugates of the invention may be convenientlyand routinely made through the well-known technique of solid-phasesynthesis. Equipment for such synthesis is sold by several vendorsincluding, for example, Applied Biosystems (Foster City, Calif.). Anyother means for such synthesis known in the art may additionally oralternatively be employed. It is also known to use similar techniques toprepare other oligonucleotides, such as the phosphorothioates andalkylated derivatives.

Teachings regarding the synthesis of particular modifiedoligonucleotides may be found in the following U.S. patents: U.S. Pat.Nos. 5,138,045 and 5,218,105, drawn to polyamine conjugatedoligonucleotides; U.S. Pat. No. 5,212,295, drawn to monomers for thepreparation of oligonucleotides having chiral phosphorus linkages; U.S.Pat. Nos. 5,378,825 and 5,541,307, drawn to oligonucleotides havingmodified backbones; U.S. Pat. No. 5,386,023, drawn to backbone-modifiedoligonucleotides and the preparation thereof through reductive coupling;U.S. Pat. No. 5,457,191, drawn to modified nucleobases based on the3-deazapurine ring system and methods of synthesis thereof; U.S. Pat.No. 5,459,255, drawn to modified nucleobases based on N-2 substitutedpurines; U.S. Pat. No. 5,521,302, drawn to processes for preparingoligonucleotides having chiral phosphorus linkages; U.S. Pat. No.5,539,082, drawn to peptide nucleic acids; U.S. Pat. No. 5,554,746,drawn to oligonucleotides having β-lactam backbones; U.S. Pat. No.5,571,902, drawn to methods and materials for the synthesis ofoligonucleotides; U.S. Pat. No. 5,578,718, drawn to nucleosides havingalkylthio groups, wherein such groups may be used as linkers to othermoieties attached at any of a variety of positions of the nucleoside;U.S. Pat. Nos. 5,587,361 and 5,599,797, drawn to oligonucleotides havingphosphorothioate linkages of high chiral purity; U.S. Pat. No.5,506,351, drawn to processes for the preparation of 2′-O-alkylguanosine and related compounds, including 2,6-diaminopurine compounds;U.S. Pat. No. 5,587,469, drawn to oligonucleotides having N-2substituted purines; U.S. Pat. No. 5,587,470, drawn to oligonucleotideshaving 3-deazapurines; U.S. Pat. No. 5,223,168, and U.S. Pat. No.5,608,046, both drawn to conjugated 4′-desmethyl nucleoside analogs;U.S. Pat. Nos. 5,602,240, and 5,610,289, drawn to backbone-modifiedoligonucleotide analogs; U.S. Pat. Nos. 6,262,241, and 5,459,255, drawnto, inter alia, methods of synthesizing 2′-fluoro-oligonucleotides.

In the ligand-conjugated dsRNA and ligand-molecule bearingsequence-specific linked nucleosides of the invention, theoligonucleotides and oligonucleosides may be assembled on a suitable DNAsynthesizer utilizing standard nucleotide or nucleoside precursors, ornucleotide or nucleoside conjugate precursors that already bear thelinking moiety, ligand-nucleotide or nucleoside-conjugate precursorsthat already bear the ligand molecule, or non-nucleoside ligand-bearingbuilding blocks.

When using nucleotide-conjugate precursors that already bear a linkingmoiety, the synthesis of the sequence-specific linked nucleosides istypically completed, and the ligand molecule is then reacted with thelinking moiety to form the ligand-conjugated oligonucleotide.Oligonucleotide conjugates bearing a variety of molecules such assteroids, vitamins, lipids and reporter molecules, has previously beendescribed (see Manoharan et al., PCT Application WO 93/07883). In apreferred embodiment, the oligonucleotides or linked nucleosides of theinvention are synthesized by an automated synthesizer usingphosphoramidites derived from ligand-nucleoside conjugates in additionto the standard phosphoramidites and non-standard phosphoramidites thatare commercially available and routinely used in oligonucleotidesynthesis.

The incorporation of a 2′-O-methyl, 2′-O-ethyl, 2′-O-propyl, 2′-O-allyl,2′-O-aminoalkyl or 2′-deoxy-2′-fluoro group in nucleosides of anoligonucleotide confers enhanced hybridization properties to theoligonucleotide. Further, oligonucleotides containing phosphorothioatebackbones have enhanced nuclease stability. Thus, functionalized, linkednucleosides of the invention can be augmented to include either or botha phosphorothioate backbone or a 2′-O-methyl, 2′-O-ethyl, 2′-O-propyl,2′-O-aminoalkyl, 2′-O-allyl or 2′-deoxy-2′-fluoro group. A summarylisting of some of the oligonucleotide modifications known in the art isfound at, for example, PCT Publication WO 200370918.

In some embodiments, functionalized nucleoside sequences of theinvention possessing an amino group at the 5′-terminus are preparedusing a DNA synthesizer, and then reacted with an active esterderivative of a selected ligand. Active ester derivatives are well knownto those skilled in the art. Representative active esters includeN-hydrosuccinimide esters, tetrafluorophenolic esters,pentafluorophenolic esters and pentachlorophenolic esters. The reactionof the amino group and the active ester produces an oligonucleotide inwhich the selected ligand is attached to the 5′-position through alinking group. The amino group at the 5′-terminus can be preparedutilizing a 5′-Amino-Modifier C6 reagent. In one embodiment, ligandmolecules may be conjugated to oligonucleotides at the 5′-position bythe use of a ligand-nucleoside phosphoramidite wherein the ligand islinked to the 5′-hydroxy group directly or indirectly via a linker. Suchligand-nucleoside phosphoramidites are typically used at the end of anautomated synthesis procedure to provide a ligand-conjugatedoligonucleotide bearing the ligand at the 5′-terminus.

Examples of modified internucleoside linkages or backbones include, forexample, phosphorothioates, chiral phosphorothioates,phosphorodithioates, phosphotriesters, aminoalkylphosphotriesters,methyl and other alkyl phosphonates including 3′-alkylene phosphonatesand chiral phosphonates, phosphinates, phosphoramidates including3′-amino phosphoramidate and aminoalkylphosphoramidates,thionophosphoramidates, thionoalkylphosphonates,thionoalkylphosphotriesters, and boranophosphates having normal 3′-5′linkages, 2′-5′ linked analogs of these, and those having invertedpolarity wherein the adjacent pairs of nucleoside units are linked 3′-5′to 5′-3′ or 2′-5′ to 5′-2′. Various salts, mixed salts and free-acidforms are also included.

Representative United States Patents relating to the preparation of theabove phosphorus-atom-containing linkages include, but are not limitedto, U.S. Pat. Nos. 3,687,808; 4,469,863; 4,476,301; 5,023,243;5,177,196; 5,188,897; 5,264,423; 5,276,019; 5,278,302; 5,286,717;5,321,131; 5,399,676; 5,405,939; 5,453,496; 5,455,233; 5,466,677;5,476,925; 5,519,126; 5,536,821; 5,541,306; 5,550,111; 5,563,253;5,571,799; 5,587,361; 5,625,050; and 5,697,248, each of which is hereinincorporated by reference.

Examples of modified internucleoside linkages or backbones that do notinclude a phosphorus atom therein (i.e., oligonucleosides) havebackbones that are formed by short chain alkyl or cycloalkyl intersugarlinkages, mixed heteroatom and alkyl or cycloalkyl intersugar linkages,or one or more short chain heteroatomic or heterocyclic intersugarlinkages. These include those having morpholino linkages (formed in partfrom the sugar portion of a nucleoside); siloxane backbones; sulfide,sulfoxide and sulfone backbones; formacetyl and thioformacetylbackbones; methylene formacetyl and thioformacetyl backbones; alkenecontaining backbones; sulfamate backbones; methyleneimino andmethylenehydrazino backbones; sulfonate and sulfonamide backbones; amidebackbones; and others having mixed N, O, S and CH₂ component parts.

Representative United States patents relating to the preparation of theabove oligonucleosides include, but are not limited to, U.S. Pat. Nos.5,034,506; 5,166,315; 5,185,444; 5,214,134; 5,216,141; 5,235,033;5,264,562; 5,264,564; 5,405,938; 5,434,257; 5,466,677; 5,470,967;5,489,677; 5,541,307; 5,561,225; 5,596,086; 5,602,240; 5,610,289;5,602,240; 5,608,046; 5,610,289; 5,618,704; 5,623,070; 5,663,312;5,633,360; 5,677,437; and 5,677,439, each of which is hereinincorporated by reference.

In certain instances, the oligonucleotide may be modified by anon-ligand group. A number of non-ligand molecules have been conjugatedto oligonucleotides in order to enhance the activity, cellulardistribution or cellular uptake of the oligonucleotide, and proceduresfor performing such conjugations are available in the scientificliterature. Such non-ligand moieties have included lipid moieties, suchas cholesterol (Letsinger et al., Proc. Natl. Acad. Sci. USA, 1989,86:6553), cholic acid (Manoharan et al., Bioorg. Med. Chem. Lett., 1994,4:1053), a thioether, e.g., hexyl-S-tritylthiol (Manoharan et al., Ann.N.Y. Acad. Sci., 1992, 660:306; Manoharan et al., Bioorg. Med. Chem.Let., 1993, 3:2765), a thiocholesterol (Oberhauser et al., Nucl. AcidsRes., 1992, 20:533), an aliphatic chain, e.g., dodecandiol or undecylresidues (Saison-Behmoaras et al., EMBO J., 1991, 10:111; Kabanov etal., FEBS Lett., 1990, 259:327; Svinarchuk et al., Biochimie, 1993,75:49), a phospholipid, e.g., di-hexadecyl-rac-glycerol ortriethylammonium 1,2-di-O-hexadecyl-rac-glycero-3-H-phosphonate(Manoharan et al., Tetrahedron Lett., 1995, 36:3651; Shea et al., Nucl.Acids Res., 1990, 18:3777), a polyamine or a polyethylene glycol chain(Manoharan et al., Nucleosides & Nucleotides, 1995, 14:969), oradamantane acetic acid (Manoharan et al., Tetrahedron Lett., 1995,36:3651), a palmityl moiety (Mishra et al., Biochim. Biophys. Acta,1995, 1264:229), or an octadecylamine orhexylamino-carbonyl-oxycholesterol moiety (Crooke et al., J. Pharmacol.Exp. Ther., 1996, 277:923). Representative United States patents thatteach the preparation of such oligonucleotide conjugates have beenlisted above. Typical conjugation protocols involve the synthesis ofoligonucleotides bearing an aminolinker at one or more positions of thesequence. The amino group is then reacted with the molecule beingconjugated using appropriate coupling or activating reagents. Theconjugation reaction may be performed either with the oligonucleotidestill bound to the solid support or following cleavage of theoligonucleotide in solution phase. Purification of the oligonucleotideconjugate by HPLC typically affords the pure conjugate. The use of acholesterol conjugate is particularly preferred since such a moiety canincrease targeting liver cells cells, a site of PCSK9 expression.

Vector Encoded RNAi Agents

The dsRNA of the invention can also be expressed from recombinant viralvectors intracellularly in vivo. The recombinant viral vectors of theinvention comprise sequences encoding the dsRNA of the invention and anysuitable promoter for expressing the dsRNA sequences. Suitable promotersinclude, for example, the U6 or H1 RNA pol III promoter sequences andthe cytomegalovirus promoter. Selection of other suitable promoters iswithin the skill in the art. The recombinant viral vectors of theinvention can also comprise inducible or regulatable promoters forexpression of the dsRNA in a particular tissue or in a particularintracellular environment. The use of recombinant viral vectors todeliver dsRNA of the invention to cells in vivo is discussed in moredetail below.

dsRNA of the invention can be expressed from a recombinant viral vectoreither as two separate, complementary RNA molecules, or as a single RNAmolecule with two complementary regions.

Any viral vector capable of accepting the coding sequences for the dsRNAmolecule(s) to be expressed can be used, for example vectors derivedfrom adenovirus (AV); adeno-associated virus (AAV); retroviruses (e.g,lentiviruses (LV), Rhabdoviruses, murine leukemia virus); herpes virus,and the like. The tropism of viral vectors can be modified bypseudotyping the vectors with envelope proteins or other surfaceantigens from other viruses, or by substituting different viral capsidproteins, as appropriate.

For example, lentiviral vectors of the invention can be pseudotyped withsurface proteins from vesicular stomatitis virus (VSV), rabies, Ebola,Mokola, and the like. AAV vectors of the invention can be made to targetdifferent cells by engineering the vectors to express different capsidprotein serotypes. For example, an AAV vector expressing a serotype 2capsid on a serotype 2 genome is called AAV 2/2. This serotype 2 capsidgene in the AAV 2/2 vector can be replaced by a serotype 5 capsid geneto produce an AAV 2/5 vector. Techniques for constructing AAV vectorswhich express different capsid protein serotypes are within the skill inthe art; see, e.g., Rabinowitz J E et al. (2002), J Virol 76:791-801,the entire disclosure of which is herein incorporated by reference.

Selection of recombinant viral vectors suitable for use in theinvention, methods for inserting nucleic acid sequences for expressingthe dsRNA into the vector, and methods of delivering the viral vector tothe cells of interest are within the skill in the art. See, for example,Dornburg R (1995), Gene Therap. 2: 301-310; Eglitis M A (1988),Biotechniques 6: 608-614; Miller A D (1990), Hum Gene Therap. 1: 5-14;Anderson W F (1998), Nature 392: 25-30; and Rubinson D A et al., Nat.Genet. 33: 401-406, the entire disclosures of which are hereinincorporated by reference.

Preferred viral vectors are those derived from AV and AAV. In aparticularly preferred embodiment, the dsRNA of the invention isexpressed as two separate, complementary single-stranded RNA moleculesfrom a recombinant AAV vector comprising, for example, either the U6 orH1 RNA promoters, or the cytomegalovirus (CMV) promoter.

A suitable AV vector for expressing the dsRNA of the invention, a methodfor constructing the recombinant AV vector, and a method for deliveringthe vector into target cells, are described in Xia H et al. (2002), Nat.Biotech. 20: 1006-1010.

Suitable AAV vectors for expressing the dsRNA of the invention, methodsfor constructing the recombinant AV vector, and methods for deliveringthe vectors into target cells are described in Samulski Ret al. (1987),J. Virol. 61: 3096-3101; Fisher K J et al. (1996), J. Virol, 70:520-532; Samulski R et al. (1989), J. Virol. 63: 3822-3826; U.S. Pat.No. 5,252,479; U.S. Pat. No. 5,139,941; International Patent ApplicationNo. WO 94/13788; and International Patent Application No. WO 93/24641,the entire disclosures of which are herein incorporated by reference.

III. Pharmaceutical Compositions Comprising dsRNA

In one embodiment, the invention provides pharmaceutical compositionscomprising a dsRNA, as described herein, and a pharmaceuticallyacceptable carrier. The pharmaceutical composition comprising the dsRNAis useful for treating a disease or disorder associated with theexpression or activity of the PCSK9 gene, such as pathological processeswhich can be mediated by down regulating PCSK9 gene expression, sucxh ashyperlipidemia. Such pharmaceutical compositions are formulated based onthe mode of delivery. One example is compositions that are formulatedfor delivery to the liver via parenteral delivery.

The pharmaceutical compositions of the invention are administered indosages sufficient to inhibit expression of the PCSK9 gene. The presentinventors have found that, because of their improved efficiency,compositions comprising the dsRNA of the invention can be administeredat surprisingly low dosages. A dosage of 5 mg dsRNA per kilogram bodyweight of recipient per day is sufficient to inhibit or suppressexpression of the PCSK9 gene and may be administered systemically to thepatient.

In general, a suitable dose of dsRNA will be in the range of 0.01 to 5.0milligrams per kilogram body weight of the recipient per day, generallyin the range of 1 microgram to 1 mg per kilogram body weight per day.The pharmaceutical composition may be administered once daily, or thedsRNA may be administered as two, three, or more sub-doses atappropriate intervals throughout the day or even using continuousinfusion or delivery through a controlled release formulation. In thatcase, the dsRNA contained in each sub-dose must be correspondinglysmaller in order to achieve the total daily dosage. The dosage unit canalso be compounded for delivery over several days, e.g., using aconventional sustained release formulation which provides sustainedrelease of the dsRNA over a several day period. Sustained releaseformulations are well known in the art.

The skilled artisan will appreciate that certain factors may influencethe dosage and timing required to effectively treat a subject, includingbut not limited to the severity of the disease or disorder, previoustreatments, the general health and/or age of the subject, and otherdiseases present. Moreover, treatment of a subject with atherapeutically effective amount of a composition can include a singletreatment or a series of treatments. Estimates of effective dosages andin vivo half-lives for the individual dsRNAs encompassed by theinvention can be made using conventional methodologies or on the basisof in vivo testing using an appropriate animal model, as describedelsewhere herein.

Advances in mouse genetics have generated a number of mouse models forthe study of various human diseases, such as pathological processeswhich can be mediated by down regulating PCSK9 gene expression. Suchmodels are used for in vivo testing of dsRNA, as well as for determininga therapeutically effective dose.

Any method can be used to administer a dsRNA of the present invention toa mammal. For example, administration can be direct; oral; or parenteral(e.g., by subcutaneous, intraventricular, intramuscular, orintraperitoneal injection, or by intravenous drip). Administration canbe rapid (e.g., by injection), or can occur over a period of time (e.g.,by slow infusion or administration of slow release formulations).

Typically, when treating a mammal with hyperlipidemia, the dsRNAmolecules are administered systemically via parental means. For example,dsRNAs, conjugated or unconjugate or formulated with or withoutliposomes, can be administered intravenously to a patient. For such, adsRNA molecule can be formulated into compositions such as sterile andnon-sterile aqueous solutions, non-aqueous solutions in common solventssuch as alcohols, or solutions in liquid or solid oil bases. Suchsolutions also can contain buffers, diluents, and other suitableadditives. For parenteral, intrathecal, or intraventricularadministration, a dsRNA molecule can be formulated into compositionssuch as sterile aqueous solutions, which also can contain buffers,diluents, and other suitable additives (e.g., penetration enhancers,carrier compounds, and other pharmaceutically acceptable carriers).

In addition, dsRNA molecules can be administered to a mammal as biologicor abiologic means as described in, for example, U.S. Pat. No.6,271,359. Abiologic delivery can be accomplished by a variety ofmethods including, without limitation, (1) loading liposomes with adsRNA acid molecule provided herein and (2) complexing a dsRNA moleculewith lipids or liposomes to form nucleic acid-lipid or nucleicacid-liposome complexes. The liposome can be composed of cationic andneutral lipids commonly used to transfect cells in vitro. Cationiclipids can complex (e.g., charge-associate) with negatively chargednucleic acids to form liposomes. Examples of cationic liposomes include,without limitation, lipofectin, lipofectamine, lipofectace, and DOTAP.Procedures for forming liposomes are well known in the art. Liposomecompositions can be formed, for example, from phosphatidylcholine,dimyristoyl phosphatidylcholine, dipalmitoyl phosphatidylcholine,dimyristoyl phosphatidylglycerol, or dioleoyl phosphatidylethanolamine.Numerous lipophilic agents are commercially available, includingLipofectin® (Invitrogen/Life Technologies, Carlsbad, Calif.) andEffectene™ (Qiagen, Valencia, Calif.). In addition, systemic deliverymethods can be optimized using commercially available cationic lipidssuch as DDAB or DOTAP, each of which can be mixed with a neutral lipidsuch as DOPE or cholesterol. In some cases, liposomes such as thosedescribed by Templeton et al. (Nature Biotechnology, 15: 647-652 (1997))can be used. In other embodiments, polycations such as polyethyleneiminecan be used to achieve delivery in vivo and ex vivo (Boletta et al., J.Am Soc. Nephrol. 7: 1728 (1996)). Additional information regarding theuse of liposomes to deliver nucleic acids can be found in U.S. Pat. No.6,271,359, PCT Publication WO 96/40964 and Morrissey, D. et al. 2005.Nat Biotechnol. 23(8):1002-7.

Biologic delivery can be accomplished by a variety of methods including,without limitation, the use of viral vectors. For example, viral vectors(e.g., adenovirus and herpesvirus vectors) can be used to deliver dsRNAmolecules to liver cells. Standard molecular biology techniques can beused to introduce one or more of the dsRNAs provided herein into one ofthe many different viral vectors previously developed to deliver nucleicacid to cells. These resulting viral vectors can be used to deliver theone or more dsRNAs to cells by, for example, infection.

dsRNAs of the present invention can be formulated in a pharmaceuticallyacceptable carrier or diluent. A “pharmaceutically acceptable carrier”(also referred to herein as an “excipient”) is a pharmaceuticallyacceptable solvent, suspending agent, or any other pharmacologicallyinert vehicle. Pharmaceutically acceptable carriers can be liquid orsolid, and can be selected with the planned manner of administration inmind so as to provide for the desired bulk, consistency, and otherpertinent transport and chemical properties. Typical pharmaceuticallyacceptable carriers include, by way of example and not limitation:water; saline solution; binding agents (e.g., polyvinylpyrrolidone orhydroxypropyl methylcellulose); fillers (e.g., lactose and other sugars,gelatin, or calcium sulfate); lubricants (e.g., starch, polyethyleneglycol, or sodium acetate); disintegrates (e.g., starch or sodium starchglycolate); and wetting agents (e.g., sodium lauryl sulfate).

In addition, dsRNA that target the PCSK9 gene can be formulated intocompositions containing the dsRNA admixed, encapsulated, conjugated, orotherwise associated with other molecules, molecular structures, ormixtures of nucleic acids. For example, a composition containing one ormore dsRNA agents that target the PCSK9 gene can contain othertherapeutic agents such as othr lipid lowering agents (e.g., statins).

Methods for Treating Diseases that Can be Modulated by Down Regulatingthe Expression of PCSK9

The methods and compositions described herein can be used to treatdiseases and conditions that can be modulated by down regulating PCSK9gene expression. For example, the compositions described herein can beused to treat hyperlipidemia and other forms of lipid inbalance such ashypercholesterolemia, hypertriglyceridemia and the pathologicalconditions associated with thiese disorders such as heart andcirculatory diseases.

Methods for Inhibiting Expression of the PCSK9 Gene

In yet another aspect, the invention provides a method for inhibitingthe expression of the PCSK9 gene in a mammal. The method comprisesadministering a composition of the invention to the mammal such thatexpression of the target PCSK9 gene is silenced. Because of their highspecificity, the dsRNAs of the invention specifically target RNAs(primary or processed) of the target PCSK9 gene. Compositions andmethods for inhibiting the expression of these PCSK9 genes using dsRNAscan be performed as described elsewhere herein.

In one embodiment, the method comprises administering a compositioncomprising a dsRNA, wherein the dsRNA comprises a nucleotide sequencewhich is complementary to at least a part of an RNA transcript of thePCSK9 gene of the mammal to be treated. When the organism to be treatedis a mammal such as a human, the composition may be administered by anymeans known in the art including, but not limited to oral or parenteralroutes, including intravenous, intramuscular, subcutaneous, transdermal,airway (aerosol) administration. In preferred embodiments, thecompositions are administered by intravenous infusion or injection.

Unless otherwise defined, all technical and scientific terms used hereinhave the same meaning as commonly understood by one of ordinary skill inthe art to which this invention belongs. Although methods and materialssimilar or equivalent to those described herein can be used in thepractice or testing of the invention, suitable methods and materials aredescribed below. All publications, patent applications, patents, andother references mentioned herein are incorporated by reference in theirentirety. In case of conflict, the present specification, includingdefinitions, will control. In addition, the materials, methods, andexamples are illustrative only and not intended to be limiting.

EXAMPLES

Gene Walking of the PCSK9 Gene

siRNA design was carried out to identify in two separate selections

a) siRNAs targeting PCSK9 human and either mouse or rat mRNA and

b) all human reactive siRNAs with predicted specificity to the targetgene PCSK9.

mRNA sequences to human, mouse and rat PCSK9 were used: Human sequenceNM_174936.2 was used as reference sequence during the complete siRNAselection procedure.

19 mer stretches conserved in human and mouse, and human and rat PCSK9mRNA sequences were identified in the first step, resulting in theselection of siRNAs crossreactive to human and mouse, and siRNAscrossreactive to human and rat targets

SiRNAs specifically targeting human PCSK9 were identified in a secondselection. All potential 19mer sequences of human PCSK9 were extractedand defined as candidate target sequences. Sequences cross-reactive tohuman, monkey, and those cross-reactive to mouse, rat, human and monkeyare all listed in Tables 1 and 2. Chemically modified versions of thosesequences and their activity in both in vitro and in vivo assays arealso listed in tables 1 and 2 and examples given in FIGS. 2-8.

In order to rank candidate target sequences and their correspondingsiRNAs and select appropriate ones, their predicted potential forinteracting with irrelevant targets (off-target potential) was taken asa ranking parameter. siRNAs with low off-target potential were definedas preferable and assumed to be more specific in vivo.

For predicting siRNA-specific off-target potential, the followingassumptions were made:

1) positions 2 to 9 (counting 5′ to 3′) of a strand (seed region) maycontribute more to off-target potential than rest of sequence (non-seedand cleavage site region)

2) positions 10 and 11 (counting 5′ to 3′) of a strand (cleavage siteregion) may contribute more to off-target potential than non-seed region

3) positions 1 and 19 of each strand are not relevant for off-targetinteractions

4) an off-target score can be calculated for each gene and each strand,based on complementarity of siRNA strand sequence to the gene's sequenceand position of mismatches

5) number of predicted off-targets as well as highest off-target scoremust be considered for off-target potential

6) off-target scores are to be considered more relevant for off-targetpotential than numbers of off-targets

7) assuming potential abortion of sense strand activity by internalmodifications introduced, only off-target potential of antisense strandwill be relevant

To identify potential off-target genes, 19mer candidate sequences weresubjected to a homology search against publically available human mRNAsequences.

The following off-target properties for each 19mer input sequence wereextracted for each off-target gene to calculate the off-target score:

Number of mismatches in non-seed region

Number of mismatches in seed region

Number of mismatches in cleavage site region

The off-target score was calculated for considering assumption 1 to 3 asfollows:

Off-target score=number of seed mismatches*10+number of cleavage sitemismatches*1.2+number of non-seed mismatches*1

The most relevant off-target gene for each siRNA corresponding to theinput 19mer sequence was defined as the gene with the lowest off-targetscore. Accordingly, the lowest off-target score was defined as therelevant off-target score for each siRNA.

dsRNA Synthesis

Source of Reagents

Where the source of a reagent is not specifically given herein, suchreagent may be obtained from any supplier of reagents for molecularbiology at a quality/purity standard for application in molecularbiology.

siRNA Synthesis

Single-stranded RNAs were produced by solid phase synthesis on a scaleof 1 μmole using an Expedite 8909 synthesizer (Applied Biosystems,Applera Deutschland GmbH, Darmstadt, Germany) and controlled pore glass(CPG, 500 Å, Proligo Biochemie GmbH, Hamburg, Germany) as solid support.RNA and RNA containing 2′-O-methyl nucleotides were generated by solidphase synthesis employing the corresponding phosphoramidites and2′-O-methyl phosphoramidites, respectively (Proligo Biochemie GmbH,Hamburg, Germany). These building blocks were incorporated at selectedsites within the sequence of the oligoribonucleotide chain usingstandard nucleoside phosphoramidite chemistry such as described inCurrent protocols in nucleic acid chemistry, Beaucage, S. L. et al.(Edrs.), John Wiley & Sons, Inc., New York, N.Y., USA. Phosphorothioatelinkages were introduced by replacement of the iodine oxidizer solutionwith a solution of the Beaucage reagent (Chruachem Ltd, Glasgow, UK) inacetonitrile (1%). Further ancillary reagents were obtained fromMallinckrodt Baker (Griesheim, Germany).

Deprotection and purification of the crude oligoribonucleotides by anionexchange HPLC were carried out according to established procedures.Yields and concentrations were determined by UV absorption of a solutionof the respective RNA at a wavelength of 260 nm using a spectralphotometer (DU 640B, Beckman Coulter GmbH, Unterschleißheim, Germany).Double stranded RNA was generated by mixing an equimolar solution ofcomplementary strands in annealing buffer (20 mM sodium phosphate, pH6.8; 100 mM sodium chloride), heated in a water bath at 85-90° C. for 3minutes and cooled to room temperature over a period of 3-4 hours. Theannealed RNA solution was stored at −20° C. until use.

For the synthesis of 3′-cholesterol-conjugated siRNAs (herein referredto as -Chol-3), an appropriately modified solid support was used for RNAsynthesis. The modified solid support was prepared as follows:

Diethyl-2-azabutane-1,4-dicarboxylate AA

A 4.7 M aqueous solution of sodium hydroxide (50 mL) was added into astirred, ice-cooled solution of ethyl glycinate hydrochloride (32.19 g,0.23 mole) in water (50 mL). Then, ethyl acrylate (23.1 g, 0.23 mole)was added and the mixture was stirred at room temperature untilcompletion of the reaction was ascertained by TLC. After 19 h thesolution was partitioned with dichloromethane (3×100 mL). The organiclayer was dried with anhydrous sodium sulfate, filtered and evaporated.The residue was distilled to afford AA (28.8 g, 61%).

3-{Ethoxycarbonylmethyl-[6-(9H-fluoren-9-ylmethoxycarbonyl-amino)-hexanoyl]-amino}-propionicacid ethyl ester AB

Fmoc-6-amino-hexanoic acid (9.12 g, 25.83 mmol) was dissolved indichloromethane (50 mL) and cooled with ice. Diisopropylcarbodiimde(3.25 g, 3.99 mL, 25.83 mmol) was added to the solution at 0° C. It wasthen followed by the addition of Diethyl-azabutane-1,4-dicarboxylate (5g, 24.6 mmol) and dimethylamino pyridine (0.305 g, 2.5 mmol). Thesolution was brought to room temperature and stirred further for 6 h.Completion of the reaction was ascertained by TLC. The reaction mixturewas concentrated under vacuum and ethyl acetate was added to precipitatediisopropyl urea. The suspension was filtered. The filtrate was washedwith 5% aqueous hydrochloric acid, 5% sodium bicarbonate and water. Thecombined organic layer was dried over sodium sulfate and concentrated togive the crude product which was purified by column chromatography (50%EtOAC/Hexanes) to yield 11.87 g (88%) of AB.

3-[(6-Amino-hexanoyl)-ethoxycarbonylmethyl-amino]-propionic acid ethylester AC

3-{Ethoxycarbonylmethyl-[6-(9H-fluoren-9-ylmethoxycarbonylamino)-hexanoyl]-amino}-propionicacid ethyl ester AB (11.5 g, 21.3 mmol) was dissolved in 20% piperidinein dimethylformamide at 0° C. The solution was continued stirring for 1h. The reaction mixture was concentrated under vacuum, water was addedto the residue, and the product was extracted with ethyl acetate. Thecrude product was purified by conversion into its hydrochloride salt.

3-({6-[17-(1,5-Dimethyl-hexyl)-10,13-dimethyl-2,3,4,7,8,9,10,11,12,13,14,15,16,17-tetradecahydro-1H-cyclopenta[a]phenanthren-3-yloxycarbonylamino]-hexanoyl}ethoxycarbonylmethyl-amino)-propionicacid ethyl ester AD

The hydrochloride salt of3-[(6-Amino-hexanoyl)-ethoxycarbonylmethyl-amino]-propionic acid ethylester AC (4.7 g, 14.8 mmol) was taken up in dichloromethane. Thesuspension was cooled to 0° C. on ice. To the suspensiondiisopropylethylamine (3.87 g, 5.2 mL, 30 mmol) was added. To theresulting solution cholesteryl chloroformate (6.675 g, 14.8 mmol) wasadded. The reaction mixture was stirred overnight. The reaction mixturewas diluted with dichloromethane and washed with 10% hydrochloric acid.The product was purified by flash chromatography (10.3 g, 92%).

1-{6-[17-(1,5-Dimethyl-hexyl)-10,13-dimethyl-2,3,4,7,8,9,10,11,12,13,14,15,16,17-tetradecahydro-1H-cyclopenta[a]phenanthren-3-yloxycarbonylamino]-hexanoyl}-4-oxo-pyrrolidine-3-carboxylicacid ethyl ester AE

Potassium t-butoxide (1.1 g, 9.8 mmol) was slurried in 30 mL of drytoluene. The mixture was cooled to 0° C. on ice and 5 g (6.6 mmol) ofdiester AD was added slowly with stirring within 20 mins. Thetemperature was kept below 5° C. during the addition. The stirring wascontinued for 30 mins at 0° C. and 1 mL of glacial acetic acid wasadded, immediately followed by 4 g of NaH₂PO₄.H₂O in 40 mL of water Theresultant mixture was extracted twice with 100 mL of dichloromethaneeach and the combined organic extracts were washed twice with 10 mL ofphosphate buffer each, dried, and evaporated to dryness. The residue wasdissolved in 60 mL of toluene, cooled to 0° C. and extracted with three50 mL portions of cold pH 9.5 carbonate buffer. The aqueous extractswere adjusted to pH 3 with phosphoric acid, and extracted with five 40mL portions of chloroform which were combined, dried and evaporated todryness. The residue was purified by column chromatography using 25%ethylacetate/hexane to afford 1.9 g of b-ketoester (39%).

[6-(3-Hydroxy-4-hydroxymethyl-pyrrolidin-1-yl)-6-oxo-hexyl]-carbamicacid17-(1,5-dimethyl-hexyl)-10,13-dimethyl-2,3,4,7,8,9,10,11,12,13,14,15,16,17-tetradecahydro-1H-cyclopenta[a]phenanthren-3-yl ester AF

Methanol (2 mL) was added dropwise over a period of 1 h to a refluxingmixture of b-ketoester AE (1.5 g, 2.2 mmol) and sodium borohydride(0.226 g, 6 mmol) in tetrahydrofuran (10 mL). Stirring was continued atreflux temperature for 1 h. After cooling to room temperature, 1 N HCl(12.5 mL) was added, the mixture was extracted with ethylacetate (3×40mL). The combined ethylacetate layer was dried over anhydrous sodiumsulfate and concentrated under vacuum to yield the product which waspurified by column chromatography (10% MeOH/CHC13) (89%).

(6-{3-[Bis-(4-methoxy-phenyl)-phenyl-methoxymethyl]-4-hydroxy-pyrrolidin-1-yl}-6-oxo-hexyl)-carbamicacid17-(1,5-dimethyl-hexyl)-10,13-dimethyl-2,3,4,7,8,9,10,11,12,13,14,15,16,17-tetradecahydro-1H-cyclopenta[a]phenanthren-3-ylester AG

Diol AF (1.25 gm 1.994 mmol) was dried by evaporating with pyridine (2×5mL) in vacuo. Anhydrous pyridine (10 mL) and4,4′-dimethoxytritylchloride (0.724 g, 2.13 mmol) were added withstirring. The reaction was carried out at room temperature overnight.The reaction was quenched by the addition of methanol. The reactionmixture was concentrated under vacuum and to the residue dichloromethane(50 mL) was added. The organic layer was washed with 1M aqueous sodiumbicarbonate. The organic layer was dried over anhydrous sodium sulfate,filtered and concentrated. The residual pyridine was removed byevaporating with toluene. The crude product was purified by columnchromatography (2% MeOH/Chloroform, Rf=0.5 in 5% MeOH/CHCl₃) (1.75 g,95%).

Succinic acidmono-(4-[bis-(4-methoxy-phenyl)-phenyl-methoxymethyl]-1-{6-[17-(1,5-dimethyl-hexyl)-10,13-dimethyl2,3,4,7,8,9,10,11,12,13,14,15,16,17-tetradecahydro-1Hcyclopenta[a]phenanthren-3-yloxycarbonylamino]-hexanoyl}-pyrrolidin-3-yl)ester AH

Compound AG (1.0 g, 1.05 mmol) was mixed with succinic anhydride (0.150g, 1.5 mmol) and DMAP (0.073 g, 0.6 mmol) and dried in a vacuum at 40°C. overnight. The mixture was dissolved in anhydrous dichloroethane (3mL), triethylamine (0.318 g, 0.440 mL, 3.15 mmol) was added and thesolution was stirred at room temperature under argon atmosphere for 16h. It was then diluted with dichloromethane (40 mL) and washed with icecold aqueous citric acid (5 wt %, 30 mL) and water (2×20 mL). Theorganic phase was dried over anhydrous sodium sulfate and concentratedto dryness. The residue was used as such for the next step.

Cholesterol Derivatised CPG AI

Succinate AH (0.254 g, 0.242 mmol) was dissolved in a mixture ofdichloromethane/acetonitrile (3:2, 3 mL). To that solution DMAP (0.0296g, 0.242 mmol) in acetonitrile (1.25 mL),2,2′-Dithio-bis(5-nitropyridine) (0.075 g, 0.242 mmol) inacetonitrile/dichloroethane (3:1, 1.25 mL) were added successively. Tothe resulting solution triphenylphosphine (0.064 g, 0.242 mmol) inacetonitrile (0.6 ml) was added. The reaction mixture turned brightorange in color. The solution was agitated briefly using a wrist-actionshaker (5 mins). Long chain alkyl amine-CPG (LCAA-CPG) (1.5 g, 61 mM)was added. The suspension was agitated for 2 h. The CPG was filteredthrough a sintered funnel and washed with acetonitrile, dichloromethaneand ether successively. Unreacted amino groups were masked using aceticanhydride/pyridine. The achieved loading of the CPG was measured bytaking UV measurement (37 mM/g).

The synthesis of siRNAs bearing a 5′-12-dodecanoic acid bisdecylamidegroup (herein referred to as “5′-C32-”) or a 5′-cholesteryl derivativegroup (herein referred to as “5′-Chol-”) was performed as described inWO 2004/065601, except that, for the cholesteryl derivative, theoxidation step was performed using the Beaucage reagent in order tointroduce a phosphorothioate linkage at the 5′-end of the nucleic acidoligomer.

Nucleic acid sequences are represented below using standardnomenclature, and specifically the abbreviations of Table 1-2.

PCSK9 siRNA Screening in HuH7 , HepG2, Hela and Primary MonkeyHepatocytes Discovers Highly Active Sequences

HuH-7cells were obtained from JCRB Cell Bank (Japanese Collection ofResearch Bioresources) (Shinjuku, Japan, cat. No.: JCRB0403) Cells werecultured in Dulbecco's MEM (Biochrom AG, Berlin, Germany, cat. No.F0435) supplemented to contain 10% fetal calf serum (FCS) (Biochrom AG,Berlin, Germany, cat. No. S0115), Penicillin 100 U/ml, Streptomycin 100μg/ml (Biochrom AG, Berlin, Germany, cat. No. A2213) and 2 mM L-Glutamin(Biochrom AG, Berlin, Germany, cat. No K0282) at 37° C. in an atmospherewith 5% CO₂ in a humidified incubator (Heraeus HERAcell, KendroLaboratory Products, Langenselbold, Germany). HepG2 and Hela cells wereobtained from American Type Culture Collection (Rockville, Md., cat. No.HB-8065) and cultured in MEM (Gibco Invitrogen, Karlsruhe, Germany, cat.No. 21090-022) supplemented to contain 10% fetal calf serum (FCS)(Biochrom AG, Berlin, Germany, cat. No. S0115), Penicillin 100 U/ml,Streptomycin 100 μg/ml (Biochrom AG, Berlin, Germany, cat. No. A2213),1× Non Essential Amino Acids (Biochrom AG, Berlin, Germany, cat. No.K-0293), and 1 mM Sodium Pyruvate (Biochrom AG, Berlin, Germany, cat.No. L-0473) at 37° C. in an atmosphere with 5% CO₂ in a humidifiedincubator (Heraeus HERAcell, Kendro Laboratory Products, Langenselbold,Germany).

For transfection with siRNA, HuH7, HepG2, or Hela cells were seeded at adensity of 2.0×10⁴ cells/well in 96-well plates and transfecteddirectly. Transfection of siRNA (30 nM for single dose screen) wascarried out with lipofectamine 2000 (Invitrogen GmbH, Karlsruhe,Germany, cat. No. 11668-019) as described by the manufacturer.

24 hours after transfection HuH7 and HepG2 cells were lysed and PCSK9mRNA levels were quantified with the Quantigene Explore Kit(Genosprectra, Dumbarton Circle Fremont, USA, cat. No. QG-000-02)according to the protocol. PCSK9 mRNA levels were normalized to GAP-DHmRNA. For each siRNA eight individual datapoints were collected. siRNAduplexes unrelated to PCSK9 gene were used as control. The activity of agiven PCSK9 specific siRNA duplex was expressed as percent PCSK9 mRNAconcentration in treated cells relative to PCSK9 mRNA concentration incells treated with the control siRNA duplex.

Primary cynomolgus monkey hepatocytes (cryopreserved) were obtained fromIn vitro Technologies, Inc. (Baltimore, Md., USA, cat No M00305) andcultured in InVitroGRO CP Medium (cat No Z99029) at 37° C. in anatmosphere with 5% CO₂ in a humidified incubator.

For transfection with siRNA, primary cynomolgus monkey cells were seededon Collagen coated plates (Fisher Scientific, cat. No. 08-774-5) at adensity of 3.5×10⁴ cells/well in 96-well plates and transfecteddirectly. Transfection of siRNA (eight 2-fold dilution series startingfrom 30 nM) in duplicates was carried out with lipofectamine 2000(Invitrogen GmbH, Karlsruhe, Germany, cat. No. 11668-019) as describedby the manufacturer.

16 hours after transfection medium was changed to fresh InVitroGRO CPMedium with Torpedo Antibiotic Mix (In vitro Technologies, Inc, cat. NoZ99000) added.

24 hours after medium change primary cynomolgus monkey cells were lysedand PCSK9 mRNA levels were quantified with the Quantigene Explore Kit(Genosprectra, Dumbarton Circle Fremont, USA, cat. No. QG-000-02)according to the protocol. PCSK9 mRNA levels were normalized to GAPDHmRNA. Normalized PCSK9/GAPDH ratios were then compared to PCSK9/GAPDHratio of lipofectamine 2000 only control.

Tables 1-2 (and FIG. 6) summarize the results and provides examples ofin vitro screens in different cell lines at different doses. Silencingof PCSK9 transcript was expressed as percentage of remaining transcriptat a given dose. Highly active sequences are those with less than 70%transcript remaining post treatment with a given siRNA at a dose lessthan or equal to 100 nm. Very active sequences are those that have lessthan 60% of transcript remaining after treatment with a dose.less thanor equal to 100 nM. Active sequences are those that have less than 85%transcript remaining after treatment with a high dose (100 nM). Examplesof active siRNA's were also screened in vivo in mouse in lipidoidformulations as described below. Active sequences in vitro were alsogenerally active in vivo (See figure FIG. 6 example).

In Vivo Efficacy Screen of PCSK9 siRNAs

Formulation Procedure

The lipidoid LNP-01.4HCl (MW 1487) (FIG. 1), Cholesterol(Sigma-Aldrich), and PEG-Ceramide C16 (Avanti Polar Lipids) were used toprepare lipid-siRNA nanoparticles. Stock solutions of each in ethanolwere prepared: LNP-01, 133 mg/mL; Cholesterol, 25 mg/mL, PEG-CeramideC16, 100 mg/mL. LNP-01, Cholesterol, and PEG-Ceramide C16 stocksolutions were then combined in a 42:48:10 molar ratio. Combined lipidsolution was mixed rapidly with aqueous siRNA (in sodium acetate pH 5)such that the final ethanol concentration was 35-45% and the finalsodium acetate concentration was 100-300 mM. Lipid-siRNA nanoparticlesformed spontaneously upon mixing. Depending on the desired particle sizedistribution, the resultant nanoparticle mixture was in some casesextruded through a polycarbonate membrane (100 nm cut-off) using athermobarrel extruder (Lipex Extruder, Northern Lipids, Inc). In othercases, the extrusion step was omitted. Ethanol removal and simultaneousbuffer exchange was accomplished by either dialysis or tangential flowfiltration. Buffer was exchanged to phosphate buffered saline (PBS) pH7.2.

Characterization of Formulations

Formulations prepared by either the standard or extrusion-free methodare characterized in a similar manner. Formulations are firstcharacterized by visual inspection. They should be whitish translucentsolutions free from aggregates or sediment. Particle size and particlesize distribution of lipid-nanoparticles are measured by dynamic lightscattering using a Malvern Zetasizer Nano ZS (Malvern, USA). Particlesshould be 20-300 nm, and ideally, 40-100 nm in size. The particle sizedistribution should be unimodal. The total siRNA concentration in theformulation, as well as the entrapped fraction, is estimated using a dyeexclusion assay. A sample of the formulated siRNA is incubated with theRNA-binding dye Ribogreen (Molecular Probes) in the presence or absenceof a formulation disrupting surfactant, 0.5% Triton-X100. The totalsiRNA in the formulation is determined by the signal from the samplecontaining the surfactant, relative to a standard curve. The entrappedfraction is determined by subtracting the “free” siRNA content (asmeasured by the signal in the absence of surfactant) from the totalsiRNA content. Percent entrapped siRNA is typically >85%.

Bolus Dosing

Bolus dosing of formulated siRNAs in C57/BL6 mice (5/group, 8-10 weeksold, Charles River Laboratories, MA) was performed by tail veininjection using a 27G needle. SiRNAs were formulated in LNP-01 (and thendialyzed against PBS) at 0.5 mg/ml concentration allowing the deliveryof the 5 mg/kg dose in 10 μl/g body weight. Mice were kept under aninfrared lamp for approximately 3 min prior to dosing to ease injection.

48 hour post dosing mice were sacrificed by CO₂-asphyxiation. 0.2 mlblood was collected by retro-orbital bleeding and the liver washarvested and frozen in liquid nitrogen. Serum and livers were stored at−80° C.

Frozen livers were grinded using 6850 Freezer/Mill Cryogenic Grinder(SPEX CentriPrep, Inc) and powders stored at −80° C. until analysis.

PCSK9 mRNA levels were detected using the branched-DNA technology basedkit from QuantiGene Reagent System (Genospectra) according to theprotocol. 10-20 mg of frozen liver powders was lysed in 600 ul of 0.16ug/ml Proteinase K (Epicentre, #MPRK092) in Tissue and Cell LysisSolution (Epicentre, #MTC096H) at 65° C. for 3hours. Then 10 ul of thelysates were added to 90 ul of Lysis Working Reagent (1 volume of stockLysis Mixture in two volumes of water) and incubated at 52° C. overnighton Genospectra capture plates with probe sets specific to mouse PCSK9and mouse GAPDH or cyclophilin B. Nucleic acid sequences for CaptureExtender (CE), Label Extender (LE) and blocking (BL) probes wereselected from the nucleic acid sequences of PCSK9, GAPDH and cyclophilinB with the help of the QuantiGene ProbeDesigner Software 2.0(Genospectra, Fremont, Calif., USA, cat. No. QG-002-02). Chemoluminescence was read on a Victor2-Light (Perkin Elmer) as Relativelight units. The ratio of PCSK9 mRNA to GAPDH or cyclophilin B mRNA inliver lysates was averaged over each treatment group and compared to acontrol group treated with PBS or a control group treated with anunrelated siRNA (blood coagulation factor VII).

Total serum cholesterol in mouse serum was measured using the StanBioCholesterol LiquiColor kit (StanBio Laboratoriy, Boerne, Tex., USA)according to manufacturer's instructions. Measurements were taken on aVictor2 1420 Multilabel Counter (Perkin Elmer) at 495 nm.

EXAMPLES

32 PCSK9 siRNAs formulated in LNP-01 liposomes were tested in vivo in amouse model. The experiment was performed at 5mg/kg siRNA dose and atleast 10 PCSK9 siRNAs showed more than 40% PCSK9 mRNA knock downcompared to a control group treated with PBS, while control grouptreated with an unrelated siRNA (blood coagulation factor VII) had noeffect (FIGS. 2-5). Silencing of PCSK9 transcript also coorelated with alowering of cholesterol in these animals (FIGS. 4-5). In addition therewas a strong coorelation between those molecules that were active invitro and those active in vivo (FIG. 6). Sequences containing differentchemical modifications were also screened in vitro (Tables 1 and 2) andin vivo. As an example, less modified sequences 9314 and 9318, and amore modified versions of that sequence 9314-(10792, 10793, and 10796);9318-(10794, 10795, 10797) were tested both in vitro (In primary monkeyhepatocytes) or in vivo (9314 and 10792) formulated in LNP-01. FIG. 7(also see Tables 1 and 2) shows that the parent molecules 9314 and 9318and the modified versions are all active in vitro. FIG. 8 as an exampleshows that both the parent 9314 and the more highly modified 10792sequences are active in vivo displaying 50-60% silencing of endogenousPCSK9 in mice. FIG. 9 furthur exemplifies that activity of otherchemically modified versions of the parents 9314 and 10792.

dsRNA Expression Vectors

In another aspect of the invention, PCSK9 specific dsRNA molecules thatmodulate PCSK9 gene expression activity are expressed from transcriptionunits inserted into DNA or RNA vectors (see, e.g., Couture, A, et al.,TIG. (1996), 12:5-10; Skillern, A., et al., International PCTPublication No. WO 00/22113, Conrad, International PCT Publication No.WO 00/22114, and Conrad, U.S. Pat. No. 6,054,299). These transgenes canbe introduced as a linear construct, a circular plasmid, or a viralvector, which can be incorporated and inherited as a transgeneintegrated into the host genome. The transgene can also be constructedto permit it to be inherited as an extrachromosomal plasmid (Gassmann,et al., Proc. Natl. Acad. Sci. USA (1995) 92:1292).

The individual strands of a dsRNA can be transcribed by promoters on twoseparate expression vectors and co-transfected into a target cell.Alternatively each individual strand of the dsRNA can be transcribed bypromoters both of which are located on the same expression plasmid. In apreferred embodiment, a dsRNA is expressed as an inverted repeat joinedby a linker polynucleotide sequence such that the dsRNA has a stem andloop structure.

The recombinant dsRNA expression vectors are generally DNA plasmids orviral vectors. dsRNA expressing viral vectors can be constructed basedon, but not limited to, adeno-associated virus (for a review, seeMuzyczka, et al., Curr. Topics Micro. Immunol. (1992) 158:97-129));adenovirus (see, for example, Berkner, et al., BioTechniques (1998)6:616), Rosenfeld et al. (1991, Science 252:431-434), and Rosenfeld etal. (1992), Cell 68:143-155)); or alphavirus as well as others known inthe art. Retroviruses have been used to introduce a variety of genesinto many different cell types, including epithelial cells, in vitroand/or in vivo (see, e.g., Eglitis, et al., Science (1985)230:1395-1398; Danos and Mulligan, Proc. Natl. Acad. Sci. USA (1998)85:6460-6464; Wilson et al., 1988, Proc. Natl. Acad. Sci. USA85:3014-3018; Armentano et al., 1990, Proc. Natl. Acad. Sci. USA87:61416145; Huber et al., 1991, Proc. Natl. Acad. Sci. USA88:8039-8043; Ferry et al., 1991, Proc. Natl. Acad. Sci. USA88:8377-8381; Chowdhury et al., 1991, Science 254:1802-1805; vanBeusechem. et al., 1992, Proc. Nad. Acad. Sci. USA 89:7640-19; Kay etal., 1992, Human Gene Therapy 3:641-647; Dai et al., 1992, Proc.Natl.Acad. Sci. USA 89:10892-10895; Hwu et al., 1993, J. Immunol.150:4104-4115; U.S. Pat. No. 4,868,116; U.S. Pat. No. 4,980,286; PCTApplication WO 89/07136; PCT Application WO 89/02468; PCT Application WO89/05345; and PCT Application WO 92/07573). Recombinant retroviralvectors capable of transducing and expressing genes inserted into thegenome of a cell can be produced by transfecting the recombinantretroviral genome into suitable packaging cell lines such as PA317 andPsi-CRIP (Comette et al., 1991, Human Gene Therapy 2:5-10; Cone et al.,1984, Proc. Natl. Acad. Sci. USA 81:6349). Recombinant adenoviralvectors can be used to infect a wide variety of cells and tissues insusceptible hosts (e.g., rat, hamster, dog, and chimpanzee) (Hsu et al.,1992, J. Infectious Disease, 166:769), and also have the advantage ofnot requiring mitotically active cells for infection.

The promoter driving dsRNA expression in either a DNA plasmid or viralvector of the invention may be a eukaryotic RNA polymerase I (e.g.ribosomal RNA promoter), RNA polymerase II (e.g. CMV early promoter oractin promoter or U1 snRNA promoter) or generally RNA polymerase IIIpromoter (e.g. U6 snRNA or 7SK RNA promoter) or a prokaryotic promoter,for example the T7 promoter, provided the expression plasmid alsoencodes T7 RNA polymerase required for transcription from a T7 promoter.The promoter can also direct transgene expression to the pancreas (see,e.g. the insulin regulatory sequence for pancreas (Bucchini et al.,1986, Proc. Natl. Acad. Sci. USA 83:2511-2515)).

In addition, expression of the transgene can be precisely regulated, forexample, by using an inducible regulatory sequence and expressionsystems such as a regulatory sequence that is sensitive to certainphysiological regulators, e.g., circulating glucose levels, or hormones(Docherty et al., 1994, FASEB J. 8:20-24). Such inducible expressionsystems, suitable for the control of transgene expression in cells or inmammals include regulation by ecdysone, by estrogen, progesterone,tetracycline, chemical inducers of dimerization, andisopropyl-beta-D1-thiogalactopyranoside (EPTG). A person skilled in theart would be able to choose the appropriate regulatory/promoter sequencebased on the intended use of the dsRNA transgene.

Generally, recombinant vectors capable of expressing dsRNA molecules aredelivered as described below, and persist in target cells.Alternatively, viral vectors can be used that provide for transientexpression of dsRNA molecules. Such vectors can be repeatedlyadministered as necessary. Once expressed, the dsRNAs bind to target RNAand modulate its function or expression. Delivery of dsRNA expressingvectors can be systemic, such as by intravenous or intramuscularadministration, by administration to target cells ex-planted from thepatient followed by reintroduction into the patient, or by any othermeans that allows for introduction into a desired target cell.

dsRNA expression DNA plasmids are typically transfected into targetcells as a complex with cationic lipid carriers (e.g. Oligofectamine) ornon-cationic lipid-based carriers (e.g. Transit-TKO™). Multiple lipidtransfections for dsRNA-mediated knockdowns targeting different regionsof a single PCSK9 gene or multiple PCSK9 genes over a period of a weekor more are also contemplated by the invention. Successful introductionof the vectors of the invention into host cells can be monitored usingvarious known methods. For example, transient transfection. can besignaled with a reporter, such as a fluorescent marker, such as GreenFluorescent Protein (GFP). Stable transfection. of ex vivo cells can beensured using markers that provide the transfected cell with resistanceto specific environmental factors (e.g., antibiotics and drugs), such ashygromycin B resistance.

The PCSK9 specific dsRNA molecules can also be inserted into vectors andused as gene therapy vectors for human patients. Gene therapy vectorscan be delivered to a subject by, for example, intravenous injection,local administration (see U.S. Patent 5,328,470) or by stereotacticinjection (see e.g., Chen et al. (1994) Proc. Natl. Acad. Sci. USA91:3054-3057). The pharmaceutical preparation of the gene therapy vectorcan include the gene therapy vector in an acceptable diluent, or cancomprise a slow release matrix in which the gene delivery vehicle isimbedded. Alternatively, where the complete gene delivery vector can beproduced intact from recombinant cells, e.g., retroviral vectors, thepharmaceutical preparation can include one or more cells which producethe gene delivery system.

Those skilled in the art are familiar with methods and compositions inaddition to those specifically set out in the instant disclosure whichwill allow them to practice this invention to the full scope of theclaims hereinafter appended.

TABLE 1  sequences position in human SEQ SEQ access. # ID ID DuplexNM_174936 Sense strand sequence (5′-3′)¹ NO:Antisense-strand sequence (5′-3′)¹ NO: name  2-20 AGCGACGUCGAGGCGCUCATT1 UGAGCGCCUCGACGUCGCUTT 2 AD-15220 15-33 CGCUCAUGGUUGCAGGCGGTT 3CCGCCUGCAACCAUGAGCGTT 4 AD-15275 16-34 GCUCAUGGUUGCAGGCGGGTT 5CCCGCCUGCAACCAUGAGCTT 6 AD-15301 30-48 GCGGGCGCCGCCGUUCAGUTT 7ACUGAACGGCGGCGCCCGCTT 8 AD-15276 31-49 CGGGCGCCGCCGUUCAGUUTT 9AACUGAACGGCGGCGCCCGTT 10 AD-15302 32-50 GGGCGCCGCCGUUCAGUUCTT 11GAACUGAACGGCGGCGCCCTT 12 AD-15303 40-58 CCGUUCAGUUCAGGGUCUGTT 13CAGACCCUGAACUGAACGGTT 14 AD-15221 43-61 UUCAGUUCAGGGUCUGAGCTT 15GCUCAGACCCUGAACUGAATT 16 AD-15413  82-100 GUGAGACUGGCUCGGGCGGTT 17CCGCCCGAGCCAGUCUCACTT 18 AD-15304 100-118 GGCCGGGACGCGUCGUUGCTT 19GCAACGACGCGUCCCGGCCTT 20 AD-15305 101-119 GCCGGGACGCGUCGUUGCATT 21UGCAACGACGCGUCCCGGCTT 22 AD-15306 102-120 CCGGGACGCGUCGUUGCAGTT 23CUGCAACGACGCGUCCCGGTT 24 AD-15307 105-123 GGACGCGUCGUUGCAGCAGTT 25CUGCUGCAACGACGCGUCCTT 26 AD-15277 135-153 UCCCAGCCAGGAUUCCGCGTsT 27CGCGGAAUCCUGGCUGGGATsT 28 AD-9526 135-153 ucccAGccAGGAuuccGcGTsT 29CGCGGAAUCCUGGCUGGGATsT 30 AD-9652 136-154 CCCAGCCAGGAUUCCGCGCTsT 31GCGCGGAAUCCUGGCUGGGTsT 32 AD-9519 136-154 cccAGccAGGAuuccGcGcTsT 33GCGCGGAAUCCUGGCUGGGTsT 34 AD-9645 138-156 CAGCCAGGAUUCCGCGCGCTsT 35GCGCGCGGAAUCCUGGCUGTsT 36 AD-9523 138-156 cAGccAGGAuuccGcGcGcTsT 37GCGCGCGGAAUCCUGGCUGTsT 38 AD-9649 185-203 AGCUCCUGCACAGUCCUCCTsT 39GGAGGACUGUGCAGGAGCUTsT 40 AD-9569 185-203 AGcuccuGcAcAGuccuccTsT 41GGAGGACUGUGcAGGAGCUTsT 42 AD-9695 205-223 CACCGCAAGGCUCAAGGCGTT 43CGCCUUGAGCCUUGCGGUGTT 44 AD-15222 208-226 CGCAAGGCUCAAGGCGCCGTT 45CGGCGCCUUGAGCCUUGCGTT 46 AD-15278 210-228 CAAGGCUCAAGGCGCCGCCTT 47GGCGGCGCCUUGAGCCUUGTT 48 AD-15178 232-250 GUGGACCGCGCACGGCCUCTT 49GAGGCCGUGCGCGGUCCACTT 50 AD-15308 233-251 UGGACCGCGCACGGCCUCUTT 51AGAGGCCGUGCGCGGUCCATT 52 AD-15223 234-252 GGACCGCGCACGGCCUCUATT 53UAGAGGCCGUGCGCGGUCCTT 54 AD-15309 235-253 GACCGCGCACGGCCUCUAGTT 55CUAGAGGCCGUGCGCGGUCTT 56 AD-15279 236-254 ACCGCGCACGGCCUCUAGGTT 57CCUAGAGGCCGUGCGCGGUTT 58 AD-15194 237-255 CCGCGCACGGCCUCUAGGUTT 59ACCUAGAGGCCGUGCGCGGTT 60 AD-15310 238-256 CGCGCACGGCCUCUAGGUCTT 61GACCUAGAGGCCGUGCGCGTT 62 AD-15311 239-257 GCGCACGGCCUCUAGGUCUTT 63AGACCUAGAGGCCGUGCGCTT 64 AD-15392 240-258 CGCACGGCCUCUAGGUCUCTT 65GAGACCUAGAGGCCGUGCGTT 66 AD-15312 248-266 CUCUAGGUCUCCUCGCCAGTT 67CUGGCGAGGAGACCUAGAGTT 68 AD-15313 249-267 UCUAGGUCUCCUCGCCAGGTT 69CCUGGCGAGGAGACCUAGATT 70 AD-15280 250-268 CUAGGUCUCCUCGCCAGGATT 71UCCUGGCGAGGAGACCUAGTT 72 AD-15267 252-270 AGGUCUCCUCGCCAGGACATT 73UGUCCUGGCGAGGAGACCUTT 74 AD-15314 258-276 CCUCGCCAGGACAGCAACCTT 75GGUUGCUGUCCUGGCGAGGTT 76 AD-15315 300-318 CGUCAGCUCCAGGCGGUCCTsT 77GGACCGCCUGGAGCUGACGTsT 78 AD-9624 300-318 cGucAGcuccAGGeGGuccTsT 79GGACCGCCUGGAGCUGACGTsT 80 AD-9750 301-319 GUCAGCUCCAGGCGGUCCUTsT 81AGGACCGCCUGGAGCUGACTsT 82 AD-9623 301-319 GucAGcuccAGaGGuccuTsT 83AGGACCGCCUGGAGCUGACTsT 84 AD-9749 370-388 GGCGCCCGUGCGCAGGAGGTT 85CCUCCUGCGCACGGGCGCCTT 86 AD-15384 408-426 GGAGCUGGUGCUAGCCUUGTsT 87CAAGGCUAGCACCAGCUCCTsT 88 AD-9607 408-426 GGAGcuGGuGcuAGccuuGTsT 89cAAGGCuAGcACcAGCUCCTsT 90 AD-9733 411-429 GCUGGUGCUAGCCUUGCGUTsT 91ACGCAAGGCUAGCACCAGCTsT 92 AD-9524 411-429 GcuGGuGcuAGccuuGcGuTsT 93ACGcAAGGCuAGcACcAGCTsT 94 AD-9650 412-430 CUGGUGCUAGCCUUGCGUUTsT 95AACGCAAGGCUAGCACCAGTsT 96 AD-9520 412-430 CUGGUGCUAGCCUUGCGUUTsT 97AACGCAAGGCUAGCACCAGTsT 98 AD-9520 412-430 cuGGuGcuAGccuuGcGuuTsT 99AACGcAAGGCuAGcACcAGTsT 100 AD-9646 416-434 UGCUAGCCUUGCGUUCCGATsT 101UCGGAACGCAAGGCUAGCATsT 102 AD-9608 416-434 uGcuAGccuuGcGuuccGATsT 103UCGGAACGcAAGGCuAGcATsT 104 AD-9734 419-437 UAGCCUUGCGUUCCGAGGATsT 105UCCUCGGAACGCAAGGCUATsT 106 AD-9546 419-437 uAGccuuGcGuuccGAGGATsT 107UCCUCGGAACGcAAGGCuATsT 108 AD-9672 439-457 GACGGCCUGGCCGAAGCACTT 109GUGCUUCGGCCAGGCCGUCTT 110 AD-15385 447-465 GGCCGAAGCACCCGAGCACTT 111GUGCUCGGGUGCUUCGGCCTT 112 AD-15393 448-466 GCCGAAGCACCCGAGCACGTT 113CGUGCUCGGGUGCUUCGGCTT 114 AD-15316 449-467 CCGAAGCACCCGAGCACGGTT 115CCGUGCUCGGGUGCUUCGGTT 116 AD-15317 458-476 CCGAGCACGGAACCACAGCTT 117GCUGUGGUUCCGUGCUCGGTT 118 AD-15318 484-502 CACCGCUGCGCCAAGGAUCTT 119GAUCCUUGGCGCAGCGGUGTT 120 AD-15195 486-504 CCGCUGCGCCAAGGAUCCGTT 121CGGAUCCUUGGCGCAGCGGTT 122 AD-15224 487-505 CGCUGCGCCAAGGAUCCGUTT 123ACGGAUCCUUGGCGCAGCGTT 124 AD-15188 489-507 CUGCGCCAAGGAUCCGUGGTT 125CCACGGAUCCUUGGCGCAGTT 126 AD-15225 500-518 AUCCGUGGAGGUUGCCUGGTT 127CCAGGCAACCUCCACGGAUTT 128 AD-15281 509-527 GGUUGCCUGGCACCUACGUTT 129ACGUAGGUGCCAGGCAACCTT 130 AD-15282 542-560 AGGAGACCCACCUCUCGCATT 131UGCGAGAGGUGGGUCUCCUTT 132 AD-15319 543-561 GGAGACCCACCUCUCGCAGTT 133CUGCGAGAGGUGGGUCUCCTT 134 AD-15226 544-562 GAGACCCACCUCUCGCAGUTT 135ACUGCGAGAGGUGGGUCUCTT 136 AD-15271 549-567 CCACCUCUCGCAGUCAGAGTT 137CUCUGACUGCGAGAGGUGGTT 138 AD-15283 552-570 CCUCUCGCAGUCAGAGCGCTT 139GCGCUCUGACUGCGAGAGGTT 140 AD-15284 553-571 CUCUCGCAGUCAGAGCGCATT 141UGCGCUCUGACUGCGAGAGTT 142 AD-15189 554-572 UCUCGCAGUCAGAGCGCACTT 143GUGCGCUCUGACUGCGAGATT 144 AD-15227 555-573 CUCGCAGUCAGAGCGCACUTsT 145AGUGCGCUCUGACUGCGAGTsT 146 AD-9547 555-573 cucGcAGucAGAGcGcAcuTsT 147AGUGCGCUCUGACUGCGAGTsT 148 AD-9673 558-576 GCAGUCAGAGCGCACUGCCTsT 149GGCAGUGCGCUCUGACUGCTsT 150 AD-9548 558-576 GcAGucAGAGcGcAcuGccTsT 151GGcAGUGCGCUCUGACUGCTsT 152 AD-9674 606-624 GGGAUACCUCACCAAGAUCTsT 153GAUCUUGGUGAGGUAUCCCTsT 154 AD-9529 606-624 GGGAuAccucAccAAGAucTsT 155GAUCUUGGUGAGGuAUCCCTsT 156 AD-9655 659-677 UGGUGAAGAUGAGUGGCGATsT 157UCGCCACUCAUCUUCACCATsT 158 AD-9605 659-677 uGGuGAAGAuGAGuGGcGATsT 159UCGCcACUcAUCUUcACcATsT 160 AD-9731 663-681 GAAGAUGAGUGGCGACCUGTsT 161CAGGUCGCCACUCAUCUUCTsT 162 AD-9596 663-681 GAAGAuGAGuGGcGAccuGTsT 163cAGGUCGCcACUcAUCUUCTsT 164 AD-9722 704-722 CCCAUGUCGACUACAUCGATsT 165UCGAUGUAGUCGACAUGGGTsT 166 AD-9583 704-722 cccAuGucGAcuAcAucGATsT 167UCGAUGuAGUCGAcAUGGGTsT 168 AD-9709 718-736 AUCGAGGAGGACUCCUCUGTsT 169CAGAGGAGUCCUCCUCGAUTsT 170 AD-9579 718-736 AucGAGGAGGAcuccucuGTsT 171cAGAGGAGUCCUCCUCGAUTsT 172 AD-9705 758-776 GGAACCUGGAGCGGAUUACTT 173GUAAUCCGCUCCAGGUUCCTT 174 AD-15394 759-777 GAACCUGGAGCGGAUUACCTT 175GGUAAUCCGCUCCAGGUUCTT 176 AD-15196 760-778 AACCUGGAGCGGAUUACCCTT 177GGGUAAUCCGCUCCAGGUUTT 178 AD-15197 777-795 CCCUCCACGGUACCGGGCGTT 179CGCCCGGUACCGUGGAGGGTT 180 AD-15198 782-800 CACGGUACCGGGCGGAUGATsT 181UCAUCCGCCCGGUACCGUGTsT 182 AD-9609 782-800 cAcGGuAccGGaGGAuGATsT 183UcAUCCGCCCGGuACCGUGTsT 184 AD-9735 783-801 ACGGUACCGGGCGGAUGAATsT 185UUCAUCCGCCCGGUACCGUTsT 186 AD-9537 783-801 AcGGuAccGGaGGAuGAATsT 187UUcAUCCGCCCGGuACCGUTsT 188 AD-9663 784-802 CGGUACCGGGCGGAUGAAUTsT 189AUUCAUCCGCCCGGUACCGTsT 190 AD-9528 784-802 cGGuAccGGGcGGAuGAAuTsT 191AUUcAUCCGCCCGGuACCGTsT 192 AD-9654 785-803 GGUACCGGGCGGAUGAAUATsT 193UAUUCAUCCGCCCGGUACCTsT 194 AD-9515 785-803 GGuAccGGaGGAuGAAuATsT 195uAUUcAUCCGCCCGGuACCTsT 196 AD-9641 786-804 GUACCGGGCGGAUGAAUACTsT 197GUAUUCAUCCGCCCGGUACTsT 198 AD-9514 786-804 GuAccGGGcGGAuGAAuAcTsT 199GuAUUcAUCCGCCCGGuACTsT 200 AD-9640 788-806 ACCGGGCGGAUGAAUACCATsT 201UGGUAUUCAUCCGCCCGGUTsT 202 AD-9530 788-806 AccGGGcGGAuGAAuAccATsT 203UGGuAUUcAUCCGCCCGGUTsT 204 AD-9656 789-807 CCGGGCGGAUGAAUACCAGTsT 205CUGGUAUUCAUCCGCCCGGTsT 206 AD-9538 789-807 ccGGaGGAuGAAuAccAGTsT 207CUGGuAUUcAUCCGCCCGGTsT 208 AD-9664 825-843 CCUGGUGGAGGUGUAUCUCTsT 209GAGAUACACCUCCACCAGGTsT 210 AD-9598 825-843 ccuGGuGGAGGuGuAucucTsT 211GAGAuAcACCUCcACcAGGTsT 212 AD-9724 826-844 CUGGUGGAGGUGUAUCUCCTsT 213GGAGAUACACCUCCACCAGTsT 214 AD-9625 826-844 cuGGuGGAGGuGuAucuccTsT 215GGAGAuAcACCUCcACcAGTsT 216 AD-9751 827-845 UGGUGGAGGUGUAUCUCCUTsT 217AGGAGAUACACCUCCACCATsT 218 AD-9556 827-845 uGGuGGAGGuGuAucuccuTsT 219AGGAGAuAcACCUCcACcATsT 220 AD-9682 828-846 GGUGGAGGUGUAUCUCCUATsT 221UAGGAGAUACACCUCCACCTsT 222 AD-9539 828-846 GGuGGAGGuGuAucuccuATsT 223uAGGAGAuAcACCUCcACCTsT 224 AD-9665 831-849 GGAGGUGUAUCUCCUAGACTsT 225GUCUAGGAGAUACACCUCCTsT 226 AD-9517 831-849 GGAGGuGuAucuccuAGAcTsT 227GUCuAGGAGAuAcACCUCCTsT 228 AD-9643 833-851 AGGUGUAUCUCCUAGACACTsT 229GUGUCUAGGAGAUACACCUTsT 230 AD-9610 833-851 AGGuGuAucuccuAGAcAcTsT 231GUGUCuAGGAGAuAcACCUTsT 232 AD-9736 833-851AfgGfuGfuAfuCfuCfcUfaGfaCfaCfTsT 233 p-gUfgUfcUfaGfgAfgAfuAfcAfcCfuTsT234 AD-14681 833-851 AGGUfGUfAUfCfUfCfCfUfAGACfACfTsT 235GUfGUfCfUfAGGAGAUfACfACfCfUfTsT 236 AD-14691 833-851AgGuGuAuCuCcUaGaCaCTsT 237 p-gUfgUfcUfaGfgAfgAfuAfcAfcCfuTsT 238AD-14701 833-851 AgGuGuAuCuCcUaGaCaCTsT 239GUfGUfCfUfAGGAGAUfACfACfCfUfTsT 240 AD-14711 833-851AfgGfuGfuAfuCfuCfcUfaGfaCfaCfTsT 241 GUGUCuaGGagAUACAccuTsT 242 AD-14721833-851 AGGUfGUfAUfCfUfCfCfUfAGACfACfTsT 243 GUGUCuaGGagAUACAccuTsT 244AD-14731 833-851 AgGuGuAuCuCcUaGaCaCTsT 245 GUGUCuaGGagAUACAccuTsT 246AD-14741 833-851 GfcAfcCfcUfcAfuAfgGfcCfuGfgAfTsT 247p-uCfcAfgGfcCfuAfuGfaGfgGfuGfcTsT 248 AD-15087 833-851GCfACfCfCfUfCfAUfAGGCfCfUfGGATsT 249 UfCfCfAGGCfCfUfAUfGAGGGUfGCfTsT 250AD-15097 833-851 GcAcCcUcAuAgGcCuGgATsT 251p-uCfcAfgGfcCfuAfuGfaGfgGfuGfcTsT 252 AD-15107 833-851GcAcCcUcAuAgGcCuGgATsT 253 UfCfCfAGGCfCfUfAUfGAGGGUfGCfTsT 254 AD-15117833-851 GfcAfcCfcUfcAfuAfgGfcCfuGfgAfTsT 255 UCCAGgcCUauGAGGGugcTsT 256AD-15127 833-851 GCfACfCfCfUfCfAUfAGGCfCfUfGGATsT 257UCCAGgcCUauGAGGGugcTsT 258 AD-15137 833-851 GcAcCcUcAuAgGcCuGgATsT 259UCCAGgcCUauGAGGGugcTsT 260 AD-15147 836-854 UGUAUCUCCUAGACACCAGTsT 261CUGGUGUCUAGGAGAUACATsT 262 AD-9516 836-854 uGuAucuccuAGAcAccAGTsT 263CUGGUGUCuAGGAGAuAcATsT 264 AD-9642 840-858 UCUCCUAGACACCAGCAUATsT 265UAUGCUGGUGUCUAGGAGATsT 266 AD-9562 840-858 ucuccuAGAcAccAGcAuATsT 267uAUGCUGGUGUCuAGGAGATsT 268 AD-9688 840-858UfcUfcCfuAfgAfcAfcCfaGfcAfuAfTsT 269 p-uAfuGfcUfgGfuGfuCfuAfgGfaGfaTsT270 AD-14677 840-858 UfCfUfCfCfUfAGACfACfCfAGCfAUfATsT 271UfAUfGCfUfGGUfGUfCfUfAGGAGATsT 272 AD-14687 840-858UcUcCuAgAcAcCaGcAuATsT 273 p-uAfuGfcUfgGfuGfuCfuAfgGfaGfaTsT 274AD-14697 840-858 UcUcCuAgAcAcCaGcAuATsT 275UfAUfGCfUfGGUfGUfCfUfAGGAGATsT 276 AD-14707 840-858UfcUfcCfuAafAfcAfcCfaGfcAfuAfTsT 277 UAUGCugGUguCUAGGagaTsT 278 AD-14717840-858 UfCfUfCfCfUfAGACfACfCfAGCfAUfATsT 279 UAUGCugGUguCUAGGagaTsT 280AD-14727 840-858 UcUcCuAgAcAcCaGcAuATsT 281 UAUGCugGUguCUAGGagaTsT 282AD-14737 840-858 AfgGfcCfuGfgAfgUfuUfaUfuCfgGfTsT 283p-cCfgAfaUfaAfaCfuCfcAfgGfcCfuTsT 284 AD-15083 840-858AGGCfCfUfGGAGUfUfUfAUfUfCfGGTsT 285 CfCfGAAUfAAACfUfCfCfAGGCfCfUfTsT 286AD-15093 840-858 AgGcCuGgAgUuUaUuCgGTsT 287p-cCfgAfaUfaAfaCfuCfcAfgGfcCfuTsT 288 AD-15103 840-858AgGcCuGgAgUuUaUuCgGTsT 289 CfCfGAAUfAAACfUfCfCfAGGCfCfUfTsT 290 AD-15113840-858 AfgGfcCfuGfgAfgUfuUfaUfuCfgGfTsT 291 CCGAAuaAAcuCCAGGccuTsT 292AD-15123 840-858 AGGCfCfUfGGAGUfUfUfAUfUfCfGGTsT 293CCGAAuaAAcuCCAGGccuTsT 294 AD-15133 840-858 AgGcCuGgAgUuUaUuCgGTsT 295CCGAAuaAAcuCCAGGccuTsT 296 AD-15143 841-859 CUCCUAGACACCAGCAUACTsT 297GUAUGCUGGUGUCUAGGAGTsT 298 AD-9521 841-859 cuccuAGAcAccAGcAuAcTsT 299GuAUGCUGGUGUCuAGGAGTsT 300 AD-9647 842-860 UCCUAGACACCAGCAUACATsT 301UGUAUGCUGGUGUCUAGGATsT 302 AD-9611 842-860 uccuAGAcAccAGcAuAcATsT 303UGuAUGCUGGUGUCuAGGATsT 304 AD-9737 843-861 CCUAGACACCAGCAUACAGTsT 305CUGUAUGCUGGUGUCUAGGTsT 306 AD-9592 843-861 ccuAGAcAccAGcAuAcAGTsT 307CUGuAUGCUGGUGUCuAGGTsT 308 AD-9718 847-865 GACACCAGCAUACAGAGUGTsT 309CACUCUGUAUGCUGGUGUCTsT 310 AD-9561 847-865 GAcAccAGcAuAcAGAGuGTsT 311cACUCUGuAUGCUGGUGUCTsT 312 AD-9687 855-873 CAUACAGAGUGACCACCGGTsT 313CCGGUGGUCACUCUGUAUGTsT 314 AD-9636 855-873 cAuAcAGAGuGAccAccGGTsT 315CCGGUGGUcACUCUGuAUGTsT 316 AD-9762 860-878 AGAGUGACCACCGGGAAAUTsT 317AUUUCCCGGUGGUCACUCUTsT 318 AD-9540 860-878 AGAGuGAccAccGGGAAAuTsT 319AUUUCCCGGUGGUcACUCUTsT 320 AD-9666 861-879 GAGUGACCACCGGGAAAUCTsT 321GAUUUCCCGGUGGUCACUCTsT 322 AD-9535 861-879 GAGuGAccAccGGGAAAucTsT 323GAUUUCCCGGUGGUcACUCTsT 324 AD-9661 863-881 GUGACCACCGGGAAAUCGATsT 325UCGAUUUCCCGGUGGUCACTsT 326 AD-9559 863-881 GuGAccAccGGGAAAucGATsT 327UCGAUUUCCCGGUGGUcACTsT 328 AD-9685 865-883 GACCACCGGGAAAUCGAGGTsT 329CCUCGAUUUCCCGGUGGUCTsT 330 AD-9533 865-883 GAccAccGGGAAAucGAGGTsT 331CCUCGAUUUCCCGGUGGUCTsT 332 AD-9659 866-884 ACCACCGGGAAAUCGAGGGTsT 333CCCUCGAUUUCCCGGUGGUTsT 334 AD-9612 866-884 AccAccGGGAAAucGAGGGTsT 335CCCUCGAUUUCCCGGUGGUTsT 336 AD-9738 867-885 CCACCGGGAAAUCGAGGGCTsT 337GCCCUCGAUUUCCCGGUGGTsT 338 AD-9557 867-885 ccAccGGGAAAucGAGGGcTsT 339GCCCUCGAUUUCCCGGUGGTsT 340 AD-9683 875-893 AAAUCGAGGGCAGGGUCAUTsT 341AUGACCCUGCCCUCGAUUUTsT 342 AD-9531 875-893 AAAucGAGGGcAGGGucAuTsT 343AUGACCCUGCCCUCGAUUUTsT 344 AD-9657 875-893AfaAfuCfgAfgGfgCfaGfgGfuCfaUfTsT 345 p-aUfgAfcCfcUfgCfcCfuCfgAfuUfuTsT346 AD-14673 875-893 AAAUfCfGAGGGCfAGGGUfCfAUfTsT 347AUfGACfCfCfUfGCfCfCfUfCfGAUfUfUfTsT 348 AD-14683 875-893AaAuCgAgGgCaGgGuCaUTsT 349 p-aUfgAfcCfcUfgCfcCfuCfgAfuUfuTsT 350AD-14693 875-893 AaAuCgAgGgCaGgGuCaUTsT 351AUfGACfCfCfUfGCfCfCfUfCfGAUfUfUfTsT 352 AD-14703 875-893AfaAfuCfgAfgGfgCfaGfgGfuCfaUfTsT 353 AUGACccUGccCUCGAuuuTsT 354 AD-14713875-893 AAAUfCfGAGGGCfAGGGUfCfAUfTsT 355 AUGACccUGccCUCGAuuuTsT 356AD-14723 875-893 AaAuCgAgGgCaGgGuCaUTsT 357 AUGACccUGccCUCGAuuuTsT 358AD-14733 875-893 CfgGfcAfcCfcUfcAfuAfgGfcCfuGfTsT 359p-cAfgGfcCfuAfuGfaGfgGfuGfcCfgTsT 360 AD-15079 875-893CfGGCfACfCfCfUfCfAUfAGGCfCfUfGTsT 361 CfAGGCfCfUfAUfGAGGGUfGCfCfGTsT 362AD-15089 875-893 CgGcAcCcUcAuAgGcCuGTsT 363p-cAfgGfcCfuAfuGfaGfgGfuGfcCfgTsT 364 AD-15099 875-893CgGcAcCcUcAuAgGcCuGTsT 365 CfAGGCfCfUfAUfGAGGGUfGCfCfGTsT 366 AD-15109875-893 CfgGfcAfcCfcUfcAfuAfgGfcCfuGfTsT 367 CAGGCcuAUgaGGGUGccgTsT 368AD-15119 875-893 CfGGCfACfCfCfUfCfAUfAGGCfCfUfGTsT 369CAGGCcuAUgaGGGUGccgTsT 370 AD-15129 875-893 CgGcAcCcUcAuAgGcCuGTsT 371CAGGCcuAUgaGGGUGccgTsT 372 AD-15139 877-895 AUCGAGGGCAGGGUCAUGGTsT 373CCAUGACCCUGCCCUCGAUTsT 374 AD-9542 877-895 AucGAGGGcAGGGucAuGGTsT 375CcAUGACCCUGCCCUCGAUTsT 376 AD-9668 878-896 cGAGGGcAGGGucAuGGucTsT 377GACcAUGACCCUGCCCUCGTsT 378 AD-9739 880-898 GAGGGCAGGGUCAUGGUCATsT 379UGACCAUGACCCUGCCCUCTsT 380 AD-9637 880-898 GAGGGcAGGGucAuGGucATsT 381UGACcAUGACCCUGCCCUCTsT 382 AD-9763 882-900 GGGCAGGGUCAUGGUCACCTsT 383GGUGACCAUGACCCUGCCCTsT 384 AD-9630 882-900 GGGcAGGGucAuGGucAccTsT 385GGUGACcAUGACCCUGCCCTsT 386 AD-9756 885-903 CAGGGUCAUGGUCACCGACTsT 387GUCGGUGACCAUGACCCUGTsT 388 AD-9593 885-903 cAGGGucAuGGucAccGAcTsT 389GUCGGUGACcAUGACCCUGTsT 390 AD-9719 886-904 AGGGUCAUGGUCACCGACUTsT 391AGUCGGUGACCAUGACCCUTsT 392 AD-9601 886-904 AGGGucAuGGucAccGAcuTsT 393AGUCGGUGACcAUGACCCUTsT 394 AD-9727 892-910 AUGGUCACCGACUUCGAGATsT 395UCUCGAAGUCGGUGACCAUTsT 396 AD-9573 892-910 AuGGucAccGAcuucGAGATsT 397UCUCGAAGUCGGUGACcAUTsT 398 AD-9699 899-917 CCGACUUCGAGAAUGUGCCTT 399GGCACAUUCUCGAAGUCGGTT 400 AD-15228 921-939 GGAGGACGGGACCCGCUUCTT 401GAAGCGGGUCCCGUCCUCCTT 402 AD-15395  993-1011 CAGCGGCCGGGAUGCCGGCTsT 403GCCGGCAUCCCGGCCGCUGTsT 404 AD-9602  993-1011 cAaGGccGGGAuGccGGcTsT 405GCCGGcAUCCCGGCCGCUGTsT 406 AD-9728 1020-1038 GGGUGCCAGCAUGCGCAGCTT 407GCUGCGCAUGCUGGCACCCTT 408 AD-15386 1038-1056 CCUGCGCGUGCUCAACUGCTsT 409GCAGUUGAGCACGCGCAGGTsT 410 AD-9580 1038-1056 ccuGcGcGuGcucAAcuGcTsT 411GcAGUUGAGcACGCGcAGGTsT 412 AD-9706 1040-1058 UGCGCGUGCUCAACUGCCATsT 413UGGCAGUUGAGCACGCGCATsT 414 AD-9581 1040-1058 uGcGcGuGcucAAcuGccATsT 415UGGcAGUUGAGcACGCGcATsT 416 AD-9707 1042-1060 CGCGUGCUCAACUGCCAAGTsT 417CUUGGCAGUUGAGCACGCGTsT 418 AD-9543 1042-1060 cGcGuGcucAAcuGccAAGTsT 419CUUGGcAGUUGAGcACGCGTsT 420 AD-9669 1053-1071 CUGCCAAGGGAAGGGCACGTsT 421CGUGCCCUUCCCUUGGCAGTsT 422 AD-9574 1053-1071 cuGccAAGGGAAGGGcAcGTsT 423CGUGCCCUUCCCUUGGcAGTsT 424 AD-9700 1057-1075 CAAGGGAAGGGCACGGUUATT 425UAACCGUGCCCUUCCCUUGTT 426 AD-15320 1058-1076 AAGGGAAGGGCACGGUUAGTT 427CUAACCGUGCCCUUCCCUUTT 428 AD-15321 1059-1077 AGGGAAGGGCACGGUUAGCTT 429GCUAACCGUGCCCUUCCCUTT 430 AD-15199 1060-1078 GGGAAGGGCACGGUUAGCGTT 431CGCUAACCGUGCCCUUCCCTT 432 AD-15167 1061-1079 GGAAGGGCACGGUUAGCGGTT 433CCGCUAACCGUGCCCUUCCTT 434 AD-15164 1062-1080 GAAGGGCACGGUUAGCGGCTT 435GCCGCUAACCGUGCCCUUCTT 436 AD-15166 1063-1081 AAGGGCACGGUUAGCGGCATT 437UGCCGCUAACCGUGCCCUUTT 438 AD-15322 1064-1082 AGGGCACGGUUAGCGGCACTT 439GUGCCGCUAACCGUGCCCUTT 440 AD-15200 1068-1086 CACGGUUAGCGGCACCCUCTT 441GAGGGUGCCGCUAACCGUGTT 442 AD-15213 1069-1087 ACGGUUAGCGGCACCCUCATT 443UGAGGGUGCCGCUAACCGUTT 444 AD-15229 1072-1090 GUUAGCGGCACCCUCAUAGTT 445CUAUGAGGGUGCCGCUAACTT 446 AD-15215 1073-1091 UUAGCGGCACCCUCAUAGGTT 447CCUAUGAGGGUGCCGCUAATT 448 AD-15214 1076-1094 GCGGCACCCUCAUAGGCCUTsT 449AGGCCUAUGAGGGUGCCGCTsT 450 AD-9315 1079-1097 GCACCCUCAUAGGCCUGGATsT 451UCCAGGCCUAUGAGGGUGCTsT 452 AD-9326 1085-1103 UCAUAGGCCUGGAGUUUAUTsT 453AUAAACUCCAGGCCUAUGATsT 454 AD-9318 1090-1108 GGCCUGGAGUUUAUUCGGATsT 455UCCGAAUAAACUCCAGGCCTsT 456 AD-9323 1091-1109 GCCUGGAGUUUAUUCGGAATsT 457UUCCGAAUAAACUCCAGGCTsT 458 AD-9314 1091-1109 GccuGGAGuuuAuucGGAATsT 459UUCCGAAuAAACUCcAGGCTsT 460 AD-10792 1091-1109 GccuGGAGuuuAuucGGAATsT 461UUCCGAAUAACUCCAGGCTsT 462 AD-10796 1093-1111 CUGGAGUUUAUUCGGAAAATsT 463UUUUCCGAAUAAACUCCAGTsT 464 AD-9638 1093-1111 cuGGAGuuuAuucGGAAAATsT 465UUUUCCGAAuAAACUCcAGTsT 466 AD-9764 1095-1113 GGAGUUUAUUCGGAAAAGCTsT 467GCUUUUCCGAAUAAACUCCTsT 468 AD-9525 1095-1113 GGAGuuuAuucGGAAAAGcTsT 469GCUUUUCCGAAuAAACUCCTsT 470 AD-9651 1096-1114 GAGUUUAUUCGGAAAAGCCTsT 471GGCUUUUCCGAAUAAACUCTsT 472 AD-9560 1096-1114 GAGuuuAuucGGAAAAGccTsT 473GGCUUUUCCGAAuAAACUCTsT 474 AD-9686 1100-1118 UUAUUCGGAAAAGCCAGCUTsT 475AGCUGGCUUUUCCGAAUAATsT 476 AD-9536 1100-1118 uuAuucGGAAAAGccAGcuTsT 477AGCUGGCUUUUCCGAAuAATsT 478 AD-9662 1154-1172 CCCUGGCGGGUGGGUACAGTsT 479CUGUACCCACCCGCCAGGGTsT 480 AD-9584 1154-1172 cccuGaGGGuGGGuAcAGTsT 481CUGuACCcACCCGCcAGGGTsT 482 AD-9710 1155-1173 CCUGGCGGGUGGGUACAGCTT 483GCUGUACCCACCCGCCAGGTT 484 AD-15323 1157-1175 UGGCGGGUGGGUACAGCCGTsT 485CGGCUGUACCCACCCGCCATsT 486 AD-9551 1157-1175 uGaGGGuGGGuAcAGccGTsT 487CGGCUGuACCcACCCGCcATsT 488 AD-9677 1158-1176 GGCGGGUGGGUACAGCCGCTT 489GCGGCUGUACCCACCCGCCTT 490 AD-15230 1162-1180 GGUGGGUACAGCCGCGUCCTT 491GGACGCGGCUGUACCCACCTT 492 AD-15231 1164-1182 UGGGUACAGCCGCGUCCUCTT 493GAGGACGCGGCUGUACCCATT 494 AD-15285 1172-1190 GCCGCGUCCUCAACGCCGCTT 495GCGGCGUUGAGGACGCGGCTT 496 AD-15396 1173-1191 CCGCGUCCUCAACGCCGCCTT 497GGCGGCGUUGAGGACGCGGTT 498 AD-15397 1216-1234 GUCGUGCUGGUCACCGCUGTsT 499CAGCGGUGACCAGCACGACTsT 500 AD-9600 1216-1234 GucGuGcuGGucAccGcuGTsT 501cAGCGGUGACcAGcACGACTsT 502 AD-9726 1217-1235 UCGUGCUGGUCACCGCUGCTsT 503GCAGCGGUGACCAGCACGATsT 504 AD-9606 1217-1235 ucGuGcuGGucAccGcuGcTsT 505GcAGCGGUGACcAGcACGATsT 506 AD-9732 1223-1241 UGGUCACCGCUGCCGGCAATsT 507UUGCCGGCAGCGGUGACCATsT 508 AD-9633 1223-1241 uGGucAccGcuGccGGcAATsT 509UUGCCGGcAGCGGUGACcATsT 510 AD-9759 1224-1242 GGUCACCGCUGCCGGCAACTsT 511GUUGCCGGCAGCGGUGACCTsT 512 AD-9588 1224-1242 GGucAccGcuGccGGcAAcTsT 513GUUGCCGGcAGCGGUGACCTsT 514 AD-9714 1227-1245 CACCGCUGCCGGCAACUUCTsT 515GAAGUUGCCGGCAGCGGUGTsT 516 AD-9589 1227-1245 cAccGcuGccGGcAAcuucTsT 517GAAGUUGCCGGcAGCGGUGTsT 518 AD-9715 1229-1247 CCGCUGCCGGCAACUUCCGTsT 519CGGAAGUUGCCGGCAGCGGTsT 520 AD-9575 1229-1247 ccGcuGccGGcAAcuuccGTsT 521CGGAAGUUGCCGGcAGCGGTsT 522 AD-9701 1230-1248 CGCUGCCGGCAACUUCCGGTsT 523CCGGAAGUUGCCGGCAGCGTsT 524 AD-9563 1230-1248 cGcuGccGGcAAcuuccGGTsT 525CCGGAAGUUGCCGGcAGCGTsT 526 AD-9689 1231-1249 GCUGCCGGCAACUUCCGGGTsT 527CCCGGAAGUUGCCGGCAGCTsT 528 AD-9594 1231-1249 GcuGccGGcAAcuuccGGGTsT 529CCCGGAAGUUGCCGGcAGCTsT 530 AD-9720 1236-1254 CGGCAACUUCCGGGACGAUTsT 531AUCGUCCCGGAAGUUGCCGTsT 532 AD-9585 1236-1254 cGGcAAcuuccGGGAcGAuTsT 533AUCGUCCCGGAAGUUGCCGTsT 534 AD-9711 1237-1255 GGCAACUUCCGGGACGAUGTsT 535CAUCGUCCCGGAAGUUGCCTsT 536 AD-9614 1237-1255 GGcAAcuuccGGGAcGAuGTsT 537cAUCGUCCCGGAAGUUGCCTsT 538 AD-9740 1243-1261 UUCCGGGACGAUGCCUGCCTsT 539GGCAGGCAUCGUCCCGGAATsT 540 AD-9615 1243-1261 uuccGGGAcGAuGccuGccTsT 541GGcAGGcAUCGUCCCGGAATsT 542 AD-9741 1248-1266 GGACGAUGCCUGCCUCUACTsT 543GUAGAGGCAGGCAUCGUCCTsT 544 AD-9534 1248-1266 GGACGAUGCCUGCCUCUACTsT 545GUAGAGGCAGGCAUCGUCCTsT 546 AD-9534 1248-1266 GGAcGAuGccuGccucuAcTsT 547GuAGAGGcAGGcAUCGUCCTsT 548 AD-9660 1279-1297 GCUCCCGAGGUCAUCACAGTT 549CUGUGAUGACCUCGGGAGCTT 550 AD-15324 1280-1298 CUCCCGAGGUCAUCACAGUTT 551ACUGUGAUGACCUCGGGAGTT 552 AD-15232 1281-1299 UCCCGAGGUCAUCACAGUUTT 553AACUGUGAUGACCUCGGGATT 554 AD-15233 1314-1332 CCAAGACCAGCCGGUGACCTT 555GGUCACCGGCUGGUCUUGGTT 556 AD-15234 1315-1333 CAAGACCAGCCGGUGACCCTT 557GGGUCACCGGCUGGUCUUGTT 558 AD-15286 1348-1366 ACCAACUUUGGCCGCUGUGTsT 559CACAGCGGCCAAAGUUGGUTsT 560 AD-9590 1348-1366 AccAAcuuuGGccGcuGuGTsT 561cAcAGCGGCcAAAGUUGGUTsT 562 AD-9716 1350-1368 CAACUUUGGCCGCUGUGUGTsT 563CACACAGCGGCCAAAGUUGTsT 564 AD-9632 1350-1368 cAAcuuuGGccGcuGuGuGTsT 565cAcAcAGCGGCcAAAGUUGTsT 566 AD-9758 1360-1378 CGCUGUGUGGACCUCUUUGTsT 567CAAAGAGGUCCACACAGCGTsT 568 AD-9567 1360-1378 cGcuGuGuGGAccucuuuGTsT 569cAAAGAGGUCcAcAcAGCGTsT 570 AD-9693 1390-1408 GACAUCAUUGGUGCCUCCATsT 571UGGAGGCACCAAUGAUGUCTsT 572 AD-9586 1390-1408 GAcAucAuuGGuGccuccATsT 573UGGAGGcACcAAUGAUGUCTsT 574 AD-9712 1394-1412 UCAUUGGUGCCUCCAGCGATsT 575UCGCUGGAGGCACCAAUGATsT 576 AD-9564 1394-1412 ucAuuGGuGccuccAGcGATsT 577UCGCUGGAGGcACcAAUGATsT 578 AD-9690 1417-1435 AGCACCUGCUUUGUGUCACTsT 579GUGACACAAAGCAGGUGCUTsT 580 AD-9616 1417-1435 AGcAccuGcuuuGuGucAcTsT 581GUGAcAcAAAGcAGGUGCUTsT 582 AD-9742 1433-1451 CACAGAGUGGGACAUCACATT 583UGUGAUGUCCCACUCUGUGTT 584 AD-15398 1486-1504 AUGCUGUCUGCCGAGCCGGTsT 585CCGGCUCGGCAGACAGCAUTsT 586 AD-9617 1486-1504 AuGcuGucuGccGAGccGGTsT 587CCGGCUCGGcAGAcAGcAUTsT 588 AD-9743 1491-1509 GUCUGCCGAGCCGGAGCUCTsT 589GAGCUCCGGCUCGGCAGACTsT 590 AD-9635 1491-1509 GucuGccGAGccGGAGcucTsT 591GAGCUCCGGCUCGGcAGACTsT 592 AD-9761 1521-1539 GUUGAGGCAGAGACUGAUCTsT 593GAUCAGUCUCUGCCUCAACTsT 594 AD-9568 1521-1539 GuuGAGGcAGAGAcuGAucTsT 595GAUcAGUCUCUGCCUcAACTsT 596 AD-9694 1527-1545 GCAGAGACUGAUCCACUUCTsT 597GAAGUGGAUCAGUCUCUGCTsT 598 AD-9576 1527-1545 GcAGAGAcuGAuccAcuucTsT 599GAAGUGGAUcAGUCUCUGCTsT 600 AD-9702 1529-1547 AGAGACUGAUCCACUUCUCTsT 601GAGAAGUGGAUCAGUCUCUTsT 602 AD-9627 1529-1547 AGAGAcuGAuccAcuucucTsT 603GAGAAGUGGAUcAGUCUCUTsT 604 AD-9753 1543-1561 UUCUCUGCCAAAGAUGUCATsT 605UGACAUCUUUGGCAGAGAATsT 606 AD-9628 1543-1561 uucucuGccAAAGAuGucATsT 607UGAcAUCUUUGGcAGAGAATsT 608 AD-9754 1545-1563 CUCUGCCAAAGAUGUCAUCTsT 609GAUGACAUCUUUGGCAGAGTsT 610 AD-9631 1545-1563 cucuGccAAAGAuGucAucTsT 611GAUGAcAUCUUUGGcAGAGTsT 612 AD-9757 1580-1598 CUGAGGACCAGCGGGUACUTsT 613AGUACCCGCUGGUCCUCAGTsT 614 AD-9595 1580-1598 cuGAGGAccAaGGGuAcuTsT 615AGuACCCGCUGGUCCUcAGTsT 616 AD-9721 1581-1599 UGAGGACCAGCGGGUACUGTsT 617CAGUACCCGCUGGUCCUCATsT 618 AD-9544 1581-1599 uGAGGAccAaGGGuAcuGTsT 619cAGuACCCGCUGGUCCUcATsT 620 AD-9670 1666-1684 ACUGUAUGGUCAGCACACUTT 621AGUGUGCUGACCAUACAGUTT 622 AD-15235 1668-1686 UGUAUGGUCAGCACACUCGTT 623CGAGUGUGCUGACCAUACATT 624 AD-15236 1669-1687 GUAUGGUCAGCACACUCGGTT 625CCGAGUGUGCUGACCAUACTT 626 AD-15168 1697-1715 GGAUGGCCACAGCCGUCGCTT 627GCGACGGCUGUGGCCAUCCTT 628 AD-15174 1698-1716 GAUGGCCACAGCCGUCGCCTT 629GGCGACGGCUGUGGCCAUCTT 630 AD-15325 1806-1824 CAAGCUGGUCUGCCGGGCCTT 631GGCCCGGCAGACCAGCUUGTT 632 AD-15326 1815-1833 CUGCCGGGCCCACAACGCUTsT 633AGCGUUGUGGGCCCGGCAGTsT 634 AD-9570 1815-1833 cuGccGGGcccAcAAcGcuTsT 635AGCGUUGUGGGCCCGGcAGTsT 636 AD-9696 1816-1834 UGCCGGGCCCACAACGCUUTsT 637AAGCGUUGUGGGCCCGGCATsT 638 AD-9566 1816-1834 uGccGGGcccAcAAcGcuuTsT 639AAGCGUUGUGGGCCCGGcATsT 640 AD-9692 1818-1836 CCGGGCCCACAACGCUUUUTsT 641AAAAGCGUUGUGGGCCCGGTsT 642 AD-9532 1818-1836 ccGGGcccAcAAcGcuuuuTsT 643AAAAGCGUUGUGGGCCCGGTsT 644 AD-9658 1820-1838 GGGCCCACAACGCUUUUGGTsT 645CCAAAAGCGUUGUGGGCCCTsT 646 AD-9549 1820-1838 GGGcccAcAAcGcuuuuGGTsT 647CcAAAAGCGUUGUGGGCCCTsT 648 AD-9675 1840-1858 GGUGAGGGUGUCUACGCCATsT 649UGGCGUAGACACCCUCACCTsT 650 AD-9541 1840-1858 GGuGAGGGuGucuAcGccATsT 651UGGCGuAGAcACCCUcACCTsT 652 AD-9667 1843-1861 GAGGGUGUCUACGCCAUUGTsT 653CAAUGGCGUAGACACCCUCTsT 654 AD-9550 1843-1861 GAGGGuGucuAcGccAuuGTsT 655cAAUGGCGuAGAcACCCUCTsT 656 AD-9676 1861-1879 GCCAGGUGCUGCCUGCUACTsT 657GUAGCAGGCAGCACCUGGCTsT 658 AD-9571 1861-1879 GccAGGuGcuGccuGcuAcTsT 659GuAGcAGGcAGcACCUGGCTsT 660 AD-9697 1862-1880 CCAGGUGCUGCCUGCUACCTsT 661GGUAGCAGGCAGCACCUGGTsT 662 AD-9572 1862-1880 ccAGGuGcuGccuGcuAccTsT 663GGuAGcAGGcAGcACCUGGTsT 664 AD-9698 2008-2026 ACCCACAAGCCGCCUGUGCTT 665GCACAGGCGGCUUGUGGGUTT 666 AD-15327 2023-2041 GUGCUGAGGCCACGAGGUCTsT 667GACCUCGUGGCCUCAGCACTsT 668 AD-9639 2023-2041 GuGcuGAGGccAcGAGGucTsT 669GACCUCGUGGCCUcAGcACTsT 670 AD-9765 2024-2042 UGCUGAGGCCACGAGGUCATsT 671UGACCUCGUGGCCUCAGCATsT 672 AD-9518 2024-2042 UGCUGAGGCCACGAGGUCATsT 673UGACCUCGUGGCCUCAGCATsT 674 AD-9518 2024-2042 uGcuGAGGccAcGAGGucATsT 675UGACCUCGUGGCCUcAGcATsT 676 AD-9644 2024-2042UfgCfuGfaGfgCfcAfcGfaGfgUfcAfTsT 677 p-uGfaCfcUfcGfuGfgCfcUfcAfgCfaTsT678 AD-14672 2024-2042 UfGCfUfGAGGCfCfACfGAGGUfCfATsT 679UfGACfCfUfCfGUfGGCfCfUfCfAGCfATsT 680 AD-14682 2024-2042UgCuGaGgCcAcGaGgUcATsT 681 p-uGfaCfcUfcGfuGfgCfcUfcAfgCfaTsT 682AD-14692 2024-2042 UgCuGaGgCcAcGaGgUcATsT 683UfGACfCfUfCfGUfGGCfCfUfCfAGCfATsT 684 AD-14702 2024-2042UfgCfuGfaGfgCfcAfcGfaGfgUfcAfTsT 685 UGACCucGUggCCUCAgcaTsT 686 AD-147122024-2042 UfGCfUfGAGGCfCfACfGAGGUfCfATsT 687 UGACCucGUggCCUCAgcaTsT 688AD-14722 2024-2042 UgCuGaGgCcAcGaGgUcATsT 689 UGACCucGUggCCUCAgcaTsT 690AD-14732 2024-2042 GfuGfgUfcAfgCfgGfcCfgGfgAfuGfTsT 691p-cAfuCfcCfgGfcCfgCfuGfaCfcAfcTsT 692 AD-15078 2024-2042GUfGGUfCfAGCfGGCfCfGGGAUfGTsT 693 CfAUfCfCfCfGGCfCfGCfUfGACfCfACfTsT 694AD-15088 2024-2042 GuGgUcAgCgGcCgGgAuGTsT 695p-cAfuCfcCfgGfcCfgCfuGfaCfcAfcTsT 696 AD-15098 2024-2042GuGgUcAgCgGcCgGgAuGTsT 697 CfAUfCfCfCfGGCfCfGCfUfGACfCfACfTsT 698AD-15108 2024-2042 GfuGfgUfcAfgCfgGfcCfgGfgAfuGfTsT 699CAUCCcgGCcgCUGACcacTsT 700 AD-15118 2024-2042GUfGGUfCfAGCfGGCfCfGGGAUfGTsT 701 CAUCCcgGCcgCUGACcacTsT 702 AD-151282024-2042 GuGgUcAgCgGcCgGgAuGTsT 703 CAUCCcgGCcgCUGACcacTsT 704 AD-151382030-2048 GGCCACGAGGUCAGCCCAATT 705 UUGGGCUGACCUCGUGGCCTT 706 AD-152372035-2053 CGAGGUCAGCCCAACCAGUTT 707 ACUGGUUGGGCUGACCUCGTT 708 AD-152872039-2057 GUCAGCCCAACCAGUGCGUTT 709 ACGCACUGGUUGGGCUGACTT 710 AD-152382041-2059 CAGCCCAACCAGUGCGUGGTT 711 CCACGCACUGGUUGGGCUGTT 712 AD-153282062-2080 CACAGGGAGGCCAGCAUCCTT 713 GGAUGCUGGCCUCCCUGUGTT 714 AD-153992072-2090 CCAGCAUCCACGCUUCCUGTsT 715 CAGGAAGCGUGGAUGCUGGTsT 716 AD-95822072-2090 ccAGcAuccAcGcuuccuGTsT 717 cAGGAAGCGUGGAUGCUGGTsT 718 AD-97082118-2136 AGUCAAGGAGCAUGGAAUCTsT 719 GAUUCCAUGCUCCUUGACUTsT 720 AD-95452118-2136 AGucAAGGAGcAuGGAAucTsT 721 GAUUCcAUGCUCCUUGACUTsT 722 AD-96712118-2136 AfgUfcAfaGfgAfgCfaUfgGfaAfuCfTsT 723p-gAfuUfcCfaUfgCfuCfcUfuGfaCfuTsT 724 AD-14674 2118-2136AGUfCfAAGGAGCfAUfGGAAUfCfTsT 725 GAUfUfCfCfAUfGCfUfCfCfUfUfGACfUfTsT 726AD-14684 2118-2136 AgUcAaGgAgCaUgGaAuCTsT 727p-gAfuUfcCfaUfgCfuCfcUfuGfaCfuTsT 728 AD-14694 2118-2136AgUcAaGgAgCaUgGaAuCTsT 729 GAUfUfCfCfAUfGCfUfCfCfUfUfGACfUfTsT 730AD-14704 2118-2136 AfgUfcAfaGfgAfgCfaUfgGfaAfuCfTsT 731GAUUCcaUGcuCCUUGacuTsT 732 AD-14714 2118-2136AGUfCfAAGGAGCfAUfGGAAUfCfTsT 733 GAUUCcaUGcuCCUUGacuTsT 734 AD-147242118-2136 AgUcAaGgAgCaUgGaAuCTsT 735 GAUUCcaUGcuCCUUGacuTsT 736 AD-147342118-2136 GfcGfgCfaCfcCfuCfaUfaGfgCfcUfTsT 737p-aGfgCfcUfaUfgAfgGfgUfgCfcGfcTsT 738 AD-15080 2118-2136GCfGGCfACfCfCfUfCfAUfAGGCfCfUfTsT 739 AGGCfCfUfAUfGAGGGUfGCfCfGCfTsT 740AD-15090 2118-2136 GeGgCaCcCuCaUaGgCcUTsT 741p-aGfgCfcUfaUfgAfgGfgUfgCfcGfcTsT 742 AD-15100 2118-2136GeGgCaCcCuCaUaGgCcUTsT 743 AGGCfCfUfAUfGAGGGUfGCfCfGCfTsT 744 AD-151102118-2136 GfcGfgCfaCfcCfuCfaUfaGfgCfcUfTsT 745 AGGCCuaUGagGGUGCcgcTsT746 AD-15120 2118-2136 GCfGGCfACfCfCfUfCfAUfAGGCfCfUfTsT 747AGGCCuaUGagGGUGCcgcTsT 748 AD-15130 2118-2136 GcGgCaCcCuCaUaGgCcUTsT 749AGGCCuaUGagGGUGCcgcTsT 750 AD-15140 2122-2140 AAGGAGCAUGGAAUCCCGGTsT 751CCGGGAUUCCAUGCUCCUUTsT 752 AD-9522 2122-2140 AAGGAGcAuGGAAucccGGTsT 753CCGGGAUUCcAUGCUCCUUTsT 754 AD-9648 2123-2141 AGGAGCAUGGAAUCCCGGCTsT 755GCCGGGAUUCCAUGCUCCUTsT 756 AD-9552 2123-2141 AGGAGcAuGGAAucccGGcTsT 757GCCGGGAUUCcAUGCUCCUTsT 758 AD-9678 2125-2143 GAGCAUGGAAUCCCGGCCCTsT 759GGGCCGGGAUUCCAUGCUCTsT 760 AD-9618 2125-2143 GAGcAuGGAAucceGGcccTsT 761GGGCCGGGAUUCcAUGCUCTsT 762 AD-9744 2230-2248 GCCUACGCCGUAGACAACATT 763UGUUGUCUACGGCGUAGGCTT 764 AD-15239 2231-2249 CCUACGCCGUAGACAACACTT 765GUGUUGUCUACGGCGUAGGTT 766 AD-15212 2232-2250 CUACGCCGUAGACAACACGTT 767CGUGUUGUCUACGGCGUAGTT 768 AD-15240 2233-2251 UACGCCGUAGACAACACGUTT 769ACGUGUUGUCUACGGCGUATT 770 AD-15177 2235-2253 CGCCGUAGACAACACGUGUTT 771ACACGUGUUGUCUACGGCGTT 772 AD-15179 2236-2254 GCCGUAGACAACACGUGUGTT 773CACACGUGUUGUCUACGGCTT 774 AD-15180 2237-2255 CCGUAGACAACACGUGUGUTT 775ACACACGUGUUGUCUACGGTT 776 AD-15241 2238-2256 CGUAGACAACACGUGUGUATT 777UACACACGUGUUGUCUACGTT 778 AD-15268 2240-2258 UAGACAACACGUGUGUAGUTT 779ACUACACACGUGUUGUCUATT 780 AD-15242 2241-2259 AGACAACACGUGUGUAGUCTT 781GACUACACACGUGUUGUCUTT 782 AD-15216 2242-2260 GACAACACGUGUGUAGUCATT 783UGACUACACACGUGUUGUCTT 784 AD-15176 2243-2261 ACAACACGUGUGUAGUCAGTT 785CUGACUACACACGUGUUGUTT 786 AD-15181 2244-2262 CAACACGUGUGUAGUCAGGTT 787CCUGACUACACACGUGUUGTT 788 AD-15243 2247-2265 CACGUGUGUAGUCAGGAGCTT 789GCUCCUGACUACACACGUGTT 790 AD-15182 2248-2266 ACGUGUGUAGUCAGGAGCCTT 791GGCUCCUGACUACACACGUTT 792 AD-15244 2249-2267 CGUGUGUAGUCAGGAGCCGTT 793CGGCUCCUGACUACACACGTT 794 AD-15387 2251-2269 UGUGUAGUCAGGAGCCGGGTT 795CCCGGCUCCUGACUACACATT 796 AD-15245 2257-2275 GUCAGGAGCCGGGACGUCATsT 797UGACGUCCCGGCUCCUGACTsT 798 AD-9555 2257-2275 GucAGGAGccGGGAcGucATsT 799UGACGUCCCGGCUCCUGACTsT 800 AD-9681 2258-2276 UCAGGAGCCGGGACGUCAGTsT 801CUGACGUCCCGGCUCCUGATsT 802 AD-9619 2258-2276 ucAGGAGccGGGAcGucAGTsT 803CUGACGUCCCGGCUCCUGATsT 804 AD-9745 2259-2277 CAGGAGCCGGGACGUCAGCTsT 805GCUGACGUCCCGGCUCCUGTsT 806 AD-9620 2259-2277 cAGGAGccGGGAcGucAGcTsT 807GCUGACGUCCCGGCUCCUGTsT 808 AD-9746 2263-2281 AGCCGGGACGUCAGCACUATT 809UAGUGCUGACGUCCCGGCUTT 810 AD-15288 2265-2283 CCGGGACGUCAGCACUACATT 811UGUAGUGCUGACGUCCCGGTT 812 AD-15246 2303-2321 CCGUGACAGCCGUUGCCAUTT 813AUGGCAACGGCUGUCACGGTT 814 AD-15289 2317-2335 GCCAUCUGCUGCCGGAGCCTsT 815GGCUCCGGCAGCAGAUGGCTsT 816 AD-9324 2375-2393 CCCAUCCCAGGAUGGGUGUTT 817ACACCCAUCCUGGGAUGGGTT 818 AD-15329 2377-2395 CAUCCCAGGAUGGGUGUCUTT 819AGACACCCAUCCUGGGAUGTT 820 AD-15330 2420-2438 AGCUUUAAAAUGGUUCCGATT 821UCGGAACCAUUUUAAAGCUTT 822 AD-15169 2421-2439 GCUUUAAAAUGGUUCCGACTT 823GUCGGAACCAUUUUAAAGCTT 824 AD-15201 2422-2440 CUUUAAAAUGGUUCCGACUTT 825AGUCGGAACCAUUUUAAAGTT 826 AD-15331 2423-2441 UUUAAAAUGGUUCCGACUUTT 827AAGUCGGAACCAUUUUAAATT 828 AD-15190 2424-2442 UUAAAAUGGUUCCGACUUGTT 829CAAGUCGGAACCAUUUUAATT 830 AD-15247 2425-2443 UAAAAUGGUUCCGACUUGUTT 831ACAAGUCGGAACCAUUUUATT 832 AD-15248 2426-2444 AAAAUGGUUCCGACUUGUCTT 833GACAAGUCGGAACCAUUUUTT 834 AD-15175 2427-2445 AAAUGGUUCCGACUUGUCCTT 835GGACAAGUCGGAACCAUUUTT 836 AD-15249 2428-2446 AAUGGUUCCGACUUGUCCCTT 837GGGACAAGUCGGAACCAUUTT 838 AD-15250 2431-2449 GGUUCCGACUUGUCCCUCUTT 839AGAGGGACAAGUCGGAACCTT 840 AD-15400 2457-2475 CUCCAUGGCCUGGCACGAGTT 841CUCGUGCCAGGCCAUGGAGTT 842 AD-15332 2459-2477 CCAUGGCCUGGCACGAGGGTT 843CCCUCGUGCCAGGCCAUGGTT 844 AD-15388 2545-2563 GAACUCACUCACUCUGGGUTT 845ACCCAGAGUGAGUGAGUUCTT 846 AD-15333 2549-2567 UCACUCACUCUGGGUGCCUTT 847AGGCACCCAGAGUGAGUGATT 848 AD-15334 2616-2634 UUUCACCAUUCAAACAGGUTT 849ACCUGUUUGAAUGGUGAAATT 850 AD-15335 2622-2640 CAUUCAAACAGGUCGAGCUTT 851AGCUCGACCUGUUUGAAUGTT 852 AD-15183 2623-2641 AUUCAAACAGGUCGAGCUGTT 853CAGCUCGACCUGUUUGAAUTT 854 AD-15202 2624-2642 UUCAAACAGGUCGAGCUGUTT 855ACAGCUCGACCUGUUUGAATT 856 AD-15203 2625-2643 UCAAACAGGUCGAGCUGUGTT 857CACAGCUCGACCUGUUUGATT 858 AD-15272 2626-2644 CAAACAGGUCGAGCUGUGCTT 859GCACAGCUCGACCUGUUUGTT 860 AD-15217 2627-2645 AAACAGGUCGAGCUGUGCUTT 861AGCACAGCUCGACCUGUUUTT 862 AD-15290 2628-2646 AACAGGUCGAGCUGUGCUCTT 863GAGCACAGCUCGACCUGUUTT 864 AD-15218 2630-2648 CAGGUCGAGCUGUGCUCGGTT 865CCGAGCACAGCUCGACCUGTT 866 AD-15389 2631-2649 AGGUCGAGCUGUGCUCGGGTT 867CCCGAGCACAGCUCGACCUTT 868 AD-15336 2633-2651 GUCGAGCUGUGCUCGGGUGTT 869CACCCGAGCACAGCUCGACTT 870 AD-15337 2634-2652 UCGAGCUGUGCUCGGGUGCTT 871GCACCCGAGCACAGCUCGATT 872 AD-15191 2657-2675 AGCUGCUCCCAAUGUGCCGTT 873CGGCACAUUGGGAGCAGCUTT 874 AD-15390 2658-2676 GCUGCUCCCAAUGUGCCGATT 875UCGGCACAUUGGGAGCAGCTT 876 AD-15338 2660-2678 UGCUCCCAAUGUGCCGAUGTT 877CAUCGGCACAUUGGGAGCATT 878 AD-15204 2663-2681 UCCCAAUGUGCCGAUGUCCTT 879GGACAUCGGCACAUUGGGATT 880 AD-15251 2665-2683 CCAAUGUGCCGAUGUCCGUTT 881ACGGACAUCGGCACAUUGGTT 882 AD-15205 2666-2684 CAAUGUGCCGAUGUCCGUGTT 883CACGGACAUCGGCACAUUGTT 884 AD-15171 2667-2685 AAUGUGCCGAUGUCCGUGGTT 885CCACGGACAUCGGCACAUUTT 886 AD-15252 2673-2691 CCGAUGUCCGUGGGCAGAATT 887UUCUGCCCACGGACAUCGGTT 888 AD-15339 2675-2693 GAUGUCCGUGGGCAGAAUGTT 889CAUUCUGCCCACGGACAUCTT 890 AD-15253 2678-2696 GUCCGUGGGCAGAAUGACUTT 891AGUCAUUCUGCCCACGGACTT 892 AD-15340 2679-2697 UCCGUGGGCAGAAUGACUUTT 893AAGUCAUUCUGCCCACGGATT 894 AD-15291 2683-2701 UGGGCAGAAUGACUUUUAUTT 895AUAAAAGUCAUUCUGCCCATT 896 AD-15341 2694-2712 ACUUUUAUUGAGCUCUUGUTT 897ACAAGAGCUCAAUAAAAGUTT 898 AD-15401 2700-2718 AUUGAGCUCUUGUUCCGUGTT 899CACGGAACAAGAGCUCAAUTT 900 AD-15342 2704-2722 AGCUCUUGUUCCGUGCCAGTT 901CUGGCACGGAACAAGAGCUTT 902 AD-15343 2705-2723 GCUCUUGUUCCGUGCCAGGTT 903CCUGGCACGGAACAAGAGCTT 904 AD-15292 2710-2728 UGUUCCGUGCCAGGCAUUCTT 905GAAUGCCUGGCACGGAACATT 906 AD-15344 2711-2729 GUUCCGUGCCAGGCAUUCATT 907UGAAUGCCUGGCACGGAACTT 908 AD-15254 2712-2730 UUCCGUGCCAGGCAUUCAATT 909UUGAAUGCCUGGCACGGAATT 910 AD-15345 2715-2733 CGUGCCAGGCAUUCAAUCCTT 911GGAUUGAAUGCCUGGCACGTT 912 AD-15206 2716-2734 GUGCCAGGCAUUCAAUCCUTT 913AGGAUUGAAUGCCUGGCACTT 914 AD-15346 2728-2746 CAAUCCUCAGGUCUCCACCTT 915GGUGGAGACCUGAGGAUUGTT 916 AD-15347 2743-2761 CACCAAGGAGGCAGGAUUCTsT 917GAAUCCUGCCUCCUUGGUGTsT 918 AD-9577 2743-2761 cAccAAGGAGGcAGGAuucTsT 919GAAUCCUGCCUCCUUGGUGTsT 920 AD-9703 2743-2761CfaCfcAfaGfgAfgGfcAfgGfaUfuCfTsT 921 p-gAfaUfcCfuGfcCfuCfcUfuGfgUfgTsT922 AD-14678 2743-2761 CfACfCfAAGGAGGCfAGGAUfUfCfTsT 923GAAUfCfCfUfGCfCfUfCfCfUfUfGGUfGTsT 924 AD-14688 2743-2761CaCcAaGgAgGcAgGaUuCTsT 925 p-gAfaUfcCfuGfcCfuCfcUfuGfgUfgTsT 926AD-14698 2743-2761 CaCcAaGgAgGcAgGaUuCTsT 927GAAUfCfCfUfGCfCfUfCfCfUfUfGGUfGTsT 928 AD-14708 2743-2761CfaCfcAfaGfgAfgGfcAfgGfaUfuCfTsT 929 GAAUCcuGCcuCCUUGgugTsT 930 AD-147182743-2761 CfACfCfAAGGAGGCfAGGAUfUfCfTsT 931 GAAUCcuGCcuCCUUGgugTsT 932AD-14728 2743-2761 CaCcAaGgAgGcAgGaUuCTsT 933 GAAUCcuGCcuCCUUGgugTsT 934AD-14738 1090-1108 GfgCfcUfgGfaGfuUMAfutIfcGfgAfTsT 935p-uCfcGfaAfuAfaAfcUfcCfaGfgCfcTsT 936 AD-15084 1090-1108GGCfCfUfGGAGUfUfUfAUfUfCfGGATsT 937 UfCfCfGAAUfAAACfUfCfCfAGGCfCfTsT 938AD-15094 1090-1108 GgCcUgGaGuUuAuUcGgATsT 939p-uCfcGfaAfuAfaAfcUfcCfaGfgCfcTsT 940 AD-15104 1090-1108GgCcUgGaGuUuAuUcGgATsT 941 UfCfCfGAAUfAAACfUfCfCfAGGCfCfTsT 942 AD-151141090-1108 GfgCfcUfgGfaGfuUfuAfuUfcGfgAfTsT 943 UCCGAauAAacUCCAGgccTsT944 AD-15124 1090-1108 GGCfCfUfGGAGUfUfUfAUfUfCfGGATsT 945UCCGAauAAacUCCAGgccTsT 946 AD-15134 1090-1108 GgCcUgGaGuUuAuUcGgATsT 947UCCGAauAAacUCCAGgccTsT 948 AD-15144 2753-2771 GCAGGAUUCUUCCCAUGGATT 949UCCAUGGGAAGAAUCCUGCTT 950 AD-15391 2794-2812 UGCAGGGACAAACAUCGUUTT 951AACGAUGUUUGUCCCUGCATT 952 AD-15348 2795-2813 GCAGGGACAAACAUCGUUGTT 953CAACGAUGUUUGUCCCUGCTT 954 AD-15349 2797-2815 AGGGACAAACAUCGUUGGGTT 955CCCAACGAUGUUUGUCCCUTT 956 AD-15170 2841-2859 CCCUCAUCUCCAGCUAACUTT 957AGUUAGCUGGAGAUGAGGGTT 958 AD-15350 2845-2863 CAUCUCCAGCUAACUGUGGTT 959CCACAGUUAGCUGGAGAUGTT 960 AD-15402 2878-2896 GCUCCCUGAUUAAUGGAGGTT 961CCUCCAUUAAUCAGGGAGCTT 962 AD-15293 2881-2899 CCCUGAUUAAUGGAGGCUUTT 963AAGCCUCCAUUAAUCAGGGTT 964 AD-15351 2882-2900 CCUGAUUAAUGGAGGCUUATT 965UAAGCCUCCAUUAAUCAGGTT 966 AD-15403 2884-2902 UGAUUAAUGGAGGCUUAGCTT 967GCUAAGCCUCCAUUAAUCATT 968 AD-15404 2885-2903 GAUUAAUGGAGGCUUAGCUTT 969AGCUAAGCCUCCAUUAAUCTT 970 AD-15207 2886-2904 AUUAAUGGAGGCUUAGCUUTT 971AAGCUAAGCCUCCAUUAAUTT 972 AD-15352 2887-2905 UUAAUGGAGGCUUAGCUUUTT 973AAAGCUAAGCCUCCAUUAATT 974 AD-15255 2903-2921 UUUCUGGAUGGCAUCUAGCTsT 975GCUAGAUGCCAUCCAGAAATsT 976 AD-9603 2903-2921 uuucuGGAuGGcAucuAGcTsT 977GCuAGAUGCcAUCcAGAAATsT 978 AD-9729 2904-2922 UUCUGGAUGGCAUCUAGCCTsT 979GGCUAGAUGCCAUCCAGAATsT 980 AD-9599 2904-2922 uucuGGAuGGcAucuAGccTsT 981GGCuAGAUGCcAUCcAGAATsT 982 AD-9725 2905-2923 UCUGGAUGGCAUCUAGCCATsT 983UGGCUAGAUGCCAUCCAGATsT 984 AD-9621 2905-2923 ucuGGAuGGcAucuAGccATsT 985UGGCuAGAUGCcAUCcAGATsT 986 AD-9747 2925-2943 AGGCUGGAGACAGGUGCGCTT 987GCGCACCUGUCUCCAGCCUTT 988 AD-15405 2926-2944 GGCUGGAGACAGGUGCGCCTT 989GGCGCACCUGUCUCCAGCCTT 990 AD-15353 2927-2945 GCUGGAGACAGGUGCGCCCTT 991GGGCGCACCUGUCUCCAGCTT 992 AD-15354 2972-2990 UUCCUGAGCCACCUUUACUTT 993AGUAAAGGUGGCUCAGGAATT 994 AD-15406 2973-2991 UCCUGAGCCACCUUUACUCTT 995GAGUAAAGGUGGCUCAGGATT 996 AD-15407 2974-2992 CCUGAGCCACCUUUACUCUTT 997AGAGUAAAGGUGGCUCAGGTT 998 AD-15355 2976-2994 UGAGCCACCUUUACUCUGCTT 999GCAGAGUAAAGGUGGCUCATT 1000 AD-15356 2978-2996 AGCCACCUUUACUCUGCUCTT 1001GAGCAGAGUAAAGGUGGCUTT 1002 AD-15357 2981-2999 CACCUUUACUCUGCUCUAUTT 1003AUAGAGCAGAGUAAAGGUGTT 1004 AD-15269 2987-3005 UACUCUGCUCUAUGCCAGGTsT1005 CCUGGCAUAGAGCAGAGUATsT 1006 AD-9565 2987-3005uAcucuGcucuAuGccAGGTsT 1007 CCUGGcAuAGAGcAGAGuATsT 1008 AD-96912998-3016 AUGCCAGGCUGUGCUAGCATT 1009 UGCUAGCACAGCCUGGCAUTT 1010 AD-153583003-3021 AGGCUGUGCUAGCAACACCTT 1011 GGUGUUGCUAGCACAGCCUTT 1012 AD-153593006-3024 CUGUGCUAGCAACACCCAATT 1013 UUGGGUGUUGCUAGCACAGTT 1014 AD-153603010-3028 GCUAGCAACACCCAAAGGUTT 1015 ACCUUUGGGUGUUGCUAGCTT 1016 AD-152193038-3056 GGAGCCAUCACCUAGGACUTT 1017 AGUCCUAGGUGAUGGCUCCTT 1018 AD-153613046-3064 CACCUAGGACUGACUCGGCTT 1019 GCCGAGUCAGUCCUAGGUGTT 1020 AD-152733051-3069 AGGACUGACUCGGCAGUGUTT 1021 ACACUGCCGAGUCAGUCCUTT 1022 AD-153623052-3070 GGACUGACUCGGCAGUGUGTT 1023 CACACUGCCGAGUCAGUCCTT 1024 AD-151923074-3092 UGGUGCAUGCACUGUCUCATT 1025 UGAGACAGUGCAUGCACCATT 1026 AD-152563080-3098 AUGCACUGUCUCAGCCAACTT 1027 GUUGGCUGAGACAGUGCAUTT 1028 AD-153633085-3103 CUGUCUCAGCCAACCCGCUTT 1029 AGCGGGUUGGCUGAGACAGTT 1030 AD-153643089-3107 CUCAGCCAACCCGCUCCACTsT 1031 GUGGAGCGGGUUGGCUGAGTsT 1032AD-9604 3089-3107 cucAGccAAcccGcuccAcTsT 1033 GUGGAGCGGGUUGGCUGAGTsT1034 AD-9730 3093-3111 GCCAACCCGCUCCACUACCTsT 1035GGUAGUGGAGCGGGUUGGCTsT 1036 AD-9527 3093-3111 GccAAcccGcuccAcuAccTsT1037 GGuAGUGGAGCGGGUUGGCTsT 1038 AD-9653 3096-3114 AACCCGCUCCACUACCCGGTT1039 CCGGGUAGUGGAGCGGGUUTT 1040 AD-15365 3099-3117 CCGCUCCACUACCCGGCAGTT1041 CUGCCGGGUAGUGGAGCGGTT 1042 AD-15294 3107-3125 CUACCCGGCAGGGUACACATT1043 UGUGUACCCUGCCGGGUAGTT 1044 AD-15173 3108-3126 UACCCGGCAGGGUACACAUTT1045 AUGUGUACCCUGCCGGGUATT 1046 AD-15366 3109-3127 ACCCGGCAGGGUACACAUUTT1047 AAUGUGUACCCUGCCGGGUTT 1048 AD-15367 3110-3128 CCCGGCAGGGUACACAUUCTT1049 GAAUGUGUACCCUGCCGGGTT 1050 AD-15257 3112-3130 CGGCAGGGUACACAUUCGCTT1051 GCGAAUGUGUACCCUGCCGTT 1052 AD-15184 3114-3132 GCAGGGUACACAUUCGCACTT1053 GUGCGAAUGUGUACCCUGCTT 1054 AD-15185 3115-3133 CAGGGUACACAUUCGCACCTT1055 GGUGCGAAUGUGUACCCUGTT 1056 AD-15258 3116-3134 AGGGUACACAUUCGCACCCTT1057 GGGUGCGAAUGUGUACCCUTT 1058 AD-15186 3196-3214 GGAACUGAGCCAGAAACGCTT1059 GCGUUUCUGGCUCAGUUCCTT 1060 AD-15274 3197-3215 GAACUGAGCCAGAAACGCATT1061 UGCGUUUCUGGCUCAGUUCTT 1062 AD-15368 3198-3216 AACUGAGCCAGAAACGCAGTT1063 CUGCGUUUCUGGCUCAGUUTT 1064 AD-15369 3201-3219 UGAGCCAGAAACGCAGAUUTT1065 AAUCUGCGUUUCUGGCUCATT 1066 AD-15370 3207-3225 AGAAACGCAGAUUGGGCUGTT1067 CAGCCCAAUCUGCGUUUCUTT 1068 AD-15259 3210-3228 AACGCAGAUUGGGCUGGCUTT1069 AGCCAGCCCAAUCUGCGUUTT 1070 AD-15408 3233-3251AGCCAAGCCUCUUCUUACUTsT 1071 AGUAAGAAGAGGCUUGGCUTsT 1072 AD-95973233-3251 AGccAAGccucuucuuAcuTsT 1073 AGuAAGAAGAGGCUUGGCUTsT 1074AD-9723 3233-3251 AfgCfcAfaGfcCfuCfuUfcUfuAfcUfTsT 1075p-aGfuAfaGfaAfgAfgGfcUfuGfgCfuTsT 1076 AD-14680 3233-3251AGCfCfAAGCfCfUfCfUfUfCfUfUfACfUfTsT 1077 AGUfAAGAAGAGGCfUfUfGGCfUfTsT1078 AD-14690 3233-3251 AgCcAaGcCuCuUcUuAcUTsT 1079p-aGfuAfaGfaAfgAfgGfcUfuGfgCfuTsT 1080 AD-14700 3233-3251AgCcAaGcCuCuUcUuAcUTsT 1081 AGUfAAGAAGAGGCfUfUfGGCfUfTsT 1082 AD-147103233-3251 AfgCfcAfaGfcCfuCfuUfcUfuAfcUfTsT 1083 AGUAAgaAGagGCUUGgcuTsT1084 AD-14720 3233-3251 AGCfCfAAGCfCfUfCfUfUfCfUfUfACfUfTsT 1085AGUAAgaAGagGCUUGgcuTsT 1086 AD-14730 3233-3251 AgCcAaGcCuCuUcUuAcUTsT1087 AGUAAgaAGagGCUUGgcuTsT 1088 AD-14740 3233-3251UfgGfuUfcCfcUfgAfgGfaCfcAfgCfTsT 1089 p-gCfuGfgUfcCfuCfaGfgGfaAfcCfaTsT1090 AD-15086 3233-3251 UfGGUfUfCfCfCfUfGAGGACfCfAGCfTsT 1091GCfUfGGUfCfCfUfCfAGGGAACfCfATsT 1092 AD-15096 3233-3251UgGuUcCcUgAgGaCcAgCTsT 1093 p-gCfuGfgUfcCfuCfaGfgGfaAfcCfaTsT 1094AD-15106 3233-3251 UgGuUcCcUgAgGaCcAgCTsT 1095GCfUfGGUfCfCfUfCfAGGGAACfCfATsT 1096 AD-15116 3233-3251UfgGfuUfcCfcUfgAfgGfaCfcAfgCfTsT 1097 GCUGGucCUcaGGGAAccaTsT 1098AD-15126 3233-3251 UfGGUfUfCfCfCfUfGAGGACfCfAGCfTsT 1099GCUGGucCUcaGGGAAccaTsT 1100 AD-15136 3233-3251 UgGuUcCcUgAgGaCcAgCTsT1101 GCUGGucCUcaGGGAAccaTsT 1102 AD-15146 3242-3260UCUUCUUACUUCACCCGGCTT 1103 GCCGGGUGAAGUAAGAAGATT 1104 AD-15260 3243-3261CUUCUUACUUCACCCGGCUTT 1105 AGCCGGGUGAAGUAAGAAGTT 1106 AD-15371 3244-3262UUCUUACUUCACCCGGCUGTT 1107 CAGCCGGGUGAAGUAAGAATT 1108 AD-15372 3262-3280GGGCUCCUCAUUUUUACGGTT 1109 CCGUAAAAAUGAGGAGCCCTT 1110 AD-15172 3263-3281GGCUCCUCAUUUUUACGGGTT 1111 CCCGUAAAAAUGAGGAGCCTT 1112 AD-15295 3264-3282GCUCCUCAUUUUUACGGGUTT 1113 ACCCGUAAAAAUGAGGAGCTT 1114 AD-15373 3265-3283CUCCUCAUUUUUACGGGUATT 1115 UACCCGUAAAAAUGAGGAGTT 1116 AD-15163 3266-3284UCCUCAUUUUUACGGGUAATT 1117 UUACCCGUAAAAAUGAGGATT 1118 AD-15165 3267-3285CCUCAUUUUUACGGGUAACTT 1119 GUUACCCGUAAAAAUGAGGTT 1120 AD-15374 3268-3286CUCAUUUUUACGGGUAACATT 1121 UGUUACCCGUAAAAAUGAGTT 1122 AD-15296 3270-3288CAUUUUUACGGGUAACAGUTT 1123 ACUGUUACCCGUAAAAAUGTT 1124 AD-15261 3271-3289AUUUUUACGGGUAACAGUGTT 1125 CACUGUUACCCGUAAAAAUTT 1126 AD-15375 3274-3292UUUACGGGUAACAGUGAGGTT 1127 CCUCACUGUUACCCGUAAATT 1128 AD-15262 3308-3326CAGACCAGGAAGCUCGGUGTT 1129 CACCGAGCUUCCUGGUCUGTT 1130 AD-15376 3310-3328GACCAGGAAGCUCGGUGAGTT 1131 CUCACCGAGCUUCCUGGUCTT 1132 AD-15377 3312-3330CCAGGAAGCUCGGUGAGUGTT 1133 CACUCACCGAGCUUCCUGGTT 1134 AD-15409 3315-3333GGAAGCUCGGUGAGUGAUGTT 1135 CAUCACUCACCGAGCUUCCTT 1136 AD-15378 3324-3342GUGAGUGAUGGCAGAACGATT 1137 UCGUUCUGCCAUCACUCACTT 1138 AD-15410 3326-3344GAGUGAUGGCAGAACGAUGTT 1139 CAUCGUUCUGCCAUCACUCTT 1140 AD-15379 3330-3348GAUGGCAGAACGAUGCCUGTT 1141 CAGGCAUCGUUCUGCCAUCTT 1142 AD-15187 3336-3354AGAACGAUGCCUGCAGGCATT 1143 UGCCUGCAGGCAUCGUUCUTT 1144 AD-15263 3339-3357ACGAUGCCUGCAGGCAUGGTT 1145 CCAUGCCUGCAGGCAUCGUTT 1146 AD-15264 3348-3366GCAGGCAUGGAACUUUUUCTT 1147 GAAAAAGUUCCAUGCCUGCTT 1148 AD-15297 3356-3374GGAACUUUUUCCGUUAUCATT 1149 UGAUAACGGAAAAAGUUCCTT 1150 AD-15208 3357-3375GAACUUUUUCCGUUAUCACTT 1151 GUGAUAACGGAAAAAGUUCTT 1152 AD-15209 3358-3376AACUUUUUCCGUUAUCACCTT 1153 GGUGAUAACGGAAAAAGUUTT 1154 AD-15193 3370-3388UAUCACCCAGGCCUGAUUCTT 1155 GAAUCAGGCCUGGGUGAUATT 1156 AD-15380 3378-3396AGGCCUGAUUCACUGGCCUTT 1157 AGGCCAGUGAAUCAGGCCUTT 1158 AD-15298 3383-3401UGAUUCACUGGCCUGGCGGTT 1159 CCGCCAGGCCAGUGAAUCATT 1160 AD-15299 3385-3403AUUCACUGGCCUGGCGGAGTT 1161 CUCCGCCAGGCCAGUGAAUTT 1162 AD-15265 3406-3424GCUUCUAAGGCAUGGUCGGTT 1163 CCGACCAUGCCUUAGAAGCTT 1164 AD-15381 3407-3425CUUCUAAGGCAUGGUCGGGTT 1165 CCCGACCAUGCCUUAGAAGTT 1166 AD-15210 3429-3447GAGGGCCAACAACUGUCCCTT 1167 GGGACAGUUGUUGGCCCUCTT 1168 AD-15270 3440-3458ACUGUCCCUCCUUGAGCACTsT 1169 GUGCUCAAGGAGGGACAGUTsT 1170 AD-95913440-3458 AcuGucccuccuuGAGcAcTsT 1171 GUGCUcAAGGAGGGAcAGUTsT 1172AD-9717 3441-3459 CUGUCCCUCCUUGAGCACCTsT 1173 GGUGCUCAAGGAGGGACAGTsT1174 AD-9622 3441-3459 cuGucccuccuuGAGcAccTsT 1175GGUGCUcAAGGAGGGAcAGTsT 1176 AD-9748 3480-3498 ACAUUUAUCUUUUGGGUCUTsT1177 AGACCCAAAAGAUAAAUGUTsT 1178 AD-9587 3480-3498AcAuuuAucuuuuGGGucuTsT 1179 AGACCcAAAAGAuAAAUGUTsT 1180 AD-97133480-3498 AfcAfuUfuAfuCfuUfuUfgGfgUfcUfTsT 1181p-aGfaCfcCfaAfaAfgAfuAfaAfuGfuTsT 1182 AD-14679 3480-3498ACfAUfUfUfAUfCfUfUfUfUfGGGUfCfUfTsT 1183 AGACfCfCfAAAAGAUfAAAUfGUfTsT1184 AD-14689 3480-3498 AcAuUuAuCuUuUgGgUcUTsT 1185p-aGfaCfcCfaAfaAfgAfuAfaAfuGfuTsT 1186 AD-14699 3480-3498AcAuUuAuCuUuUgGgUcUTsT 1187 AGACfCfCfAAAAGAUfAAAUfGUfTsT 1188 AD-147093480-3498 AfcAfuUfuAfuCfuUfuUfgGfgUfcUfTsT 1189 AGACCcaAAagAUAAAuguTsT1190 AD-14719 3480-3498 ACfAUfUfUfAUfCfUfUfUfUfGGGUfCfUfTsT 1191AGACCcaAAagAUAAAuguTsT 1192 AD-14729 3480-3498 AcAuUuAuCuUuUgGgUcUTsT1193 AGACCcaAAagAUAAAuguTsT 1194 AD-14739 3480-3498GfcCfaUfcUfgCfuGfcCfgGfaGfcCfTsT 1195 p-gGfcUfcCfgGfcAfgCfaGfaUfgGfcTsT1196 AD-15085 3480-3498 GCfCfAUfCfUfGCfUfGCfCfGGAGCfCfTsT 1197GGCfUfCfCfGGCfAGCfAGAUfGGCfTsT 1198 AD-15095 3480-3498GcCaUcUgCuGcCgGaGcCTsT 1199 p-gGfcUfcCfgGfcAfgCfaGfaUfgGfcTsT 1200AD-15105 3480-3498 GcCaUcUgCuGcCgGaGcCTsT 1201GGCfUfCfCfGGCfAGCfAGAUfGGCfTsT 1202 AD-15115 3480-3498GfcCfaUfcUfgCfuGfcCfgGfaGfcCfTsT 1203 GGCUCauGCagCAGAUggcTsT 1204AD-15125 3480-3498 GCfCfAUfCfUfGCfUfGCfCfGGAGCfCfTsT 1205GGCUCauGCagCAGAUggcTsT 1206 AD-15135 3480-3498 GcCaUcUgCuGcCgGaGcCTsT1207 GGCUCauGCagCAGAUggcTsT 1208 AD-15145 3481-3499CAUUUAUCUUUUGGGUCUGTsT 1209 CAGACCCAAAAGAUAAAUGTsT 1210 AD-95783481-3499 cAuuuAucuuuuGGGucuGTsT 1211 cAGACCcAAAAGAuAAAUGTsT 1212AD-9704 3485-3503 UAUCUUUUGGGUCUGUCCUTsT 1213 AGGACAGACCCAAAAGAUATsT1214 AD-9558 3485-3503 uAucuuuuGGGucuGuccuTsT 1215AGGAcAGACCcAAAAGAuATsT 1216 AD-9684 3504-3522 CUCUGUUGCCUUUUUACAGTsT1217 CUGUAAAAAGGCAACAGAGTsT 1218 AD-9634 3504-3522cucuGuuGccuuuuuAcAGTsT 1219 CUGuAAAAAGGcAAcAGAGTsT 1220 AD-97603512-3530 CCUUUUUACAGCCAACUUUTT 1221 AAAGUUGGCUGUAAAAAGGTT 1222 AD-154113521-3539 AGCCAACUUUUCUAGACCUTT 1223 AGGUCUAGAAAAGUUGGCUTT 1224 AD-152663526-3544 ACUUUUCUAGACCUGUUUUTT 1225 AAAACAGGUCUAGAAAAGUTT 1226 AD-153823530-3548 UUCUAGACCUGUUUUGCUUTsT 1227 AAGCAAAACAGGUCUAGAATsT 1228AD-9554 3530-3548 uucuAGAccuGuuuuGcuuTsT 1229 AAGcAAAAcAGGUCuAGAATsT1230 AD-9680 3530-3548 UfuCfuAfgAfcCfuGfuUfuUfgCfuUfTsT 1231p-aAfgCfaAfaAfcAfgGfuCfuAfgAfaTsT 1232 AD-14676 3530-3548UfUfCfUfAGACfCfUfGUfUfUfUfGCfUfUfTsT 1233 AAGCfAAAACfAGGUfCfUfAGAATsT1234 AD-14686 3530-3548 UuCuAgAcCuGuUuUgCuUTsT 1235p-aAfgCfaAfaAfcAfgGfuCfuAfgAfaTsT 1236 AD-14696 3530-3548UuCuAgAcCuGuUuUgCuUTsT 1237 AAGCfAAAACfAGGUfCfUfAGAATsT 1238 AD-147063530-3548 UfuCfuAfgAfcCfuGfuUfuUffCfuUfTsT 1239 AAGcAaaACagGUCUAgaaTsT1240 AD-14716 3530-3548 UfUfCfUfAGACfCfUfGUfUfUfUfGCfUfUfTsT 1241AAGcAaaACagGUCUAgaaTsT 1242 AD-14726 3530-3548 UuCuAgAcCuGuUuUgCuUTsT1243 AAGcAaaACagGUCUAgaaTsT 1244 AD-14736 3530-3548CfaUfaGfgCfcUfgGfaGfuUfuAfuUfTsT 1245 p-aAfuAfaAfcUfcCfaGfgCfcUfaUfgTsT1246 AD-15082 3530-3548 CfAUfAGGCfCfUfGGAGUfUfUfAUfUfTsT 1247AAUfAAACfUfCfCfAGGCfCfUfAUfGTsT 1248 AD-15092 3530-3548CaUaGgCcUgGaGuUuAuUTsT 1249 p-aAfuAfaAfcUfcCfaGfgCfcUfaUfgTsT 1250AD-15102 3530-3548 CaUaGgCcUgGaGuUuAuUTsT 1251AAUfAAACfUfCfCfAGGCfCfUfAUfGTsT 1252 AD-15112 3530-3548CfaUfaGfgCfcUfgGfaGfuUfuAfuUfTsT 1253 AAUAAacUCcaGGCCUaugTsT 1254AD-15122 3530-3548 CfAUfAGGCfCfUfGGAGUfUfUfAUfUfTsT 1255AAUAAacUCcaGGCCUaugTsT 1256 AD-15132 3530-3548 CaUaGgCcUgGaGuUuAuUTsT1257 AAUAAacUCcaGGCCUaugTsT 1258 AD-15142 3531-3549UCUAGACCUGUUUUGCUUUTsT 1259 AAAGCAAAACAGGUCUAGATsT 1260 AD-95533531-3549 ucuAGAccuGuuuuGcuuuTsT 1261 AAAGcAAAAcAGGUCuAGATsT 1262AD-9679 3531-3549 UfcUfaGfaCfcUfgUfuUfuGfcUfuUfTsT 1263p-aAfaGfcAfaAfaCfaGfgUfcUfaGfaTsT 1264 AD-14675 3531-3549UfCfUfAGACfCfUfGUfUfUfUfGCfUfUfUfTsT 1265 AAAGCfAAAACfAGGUfCfUfAGATsT1266 AD-14685 3531-3549 UcUaGaCcUgUuUuGcUuUTsT 1267p-aAfaGfcAfaAfaCfaGfgUfcUfaGfaTsT 1268 AD-14695 3531-3549UcUaGaCcUgUuUuGcUuUTsT 1269 AAAGCfAAAACfAGGUfCfUfAGATsT 1270 AD-147053531-3549 UfcUfaGfaCfcUfgUfuUfuGfcUfuUfTsT 1271 AAAGCaaAAcaGGUCUagaTsT1272 AD-14715 3531-3549 UfCfUfAGACfCfUfGUfUfUfUfGCfUfUfUfTsT 1273AAAGCaaAAcaGGUCUagaTsT 1274 AD-14725 3531-3549 UcUaGaCcUgUuUuGcUuUTsT1275 AAAGCaaAAcaGGUCUagaTsT 1276 AD-14735 3531-3549UfcAfuAfgGfcCfuGfgAfgUfuUfaUfTsT 1277 p-aUfaAfaCfuCfcAfgGfcCfuAfuGfaTsT1278 AD-15081 3531-3549 UfCfAUfAGGCfCfUfGGAGUfUfUfAUfTsT 1279AUfAAACfUfCfCfAGGCfCfUfAUfGATsT 1280 AD-15091 3531-3549UcAuAgGcCuGgAgUuUaUTsT 1281 p-aUfaAfaCfuCfcAfgGfcCfuAfuGfaTsT 1282AD-15101 3531-3549 UcAuAgGcCuGgAgUuUaUTsT 1283AUfAAACfUfCfCfAGGCfCfUfAUfGATsT 1284 AD-15111 3531-3549UfcAfuAfgGfcCfuGfgAfgUfuUfaUfTsT 1285 AUAAAcuCCagGCCUAugaTsT 1286AD-15121 3531-3549 UfCfAUfAGGCfCfUfGGAGUfUfUfAUfTsT 1287AUAAAcuCCagGCCUAugaTsT 1288 AD-15131 3531-3549 UcAuAgGcCuGgAgUuUaUTsT1289 AUAAAcuCCagGCCUAugaTsT 1290 AD-15141 3557-3575UGAAGAUAUUUAUUCUGGGTsT 1291 CCCAGAAUAAAUAUCUUCATsT 1292 AD-96263557-3575 uGAAGAuAuuuAuucuGGGTsT 1293 CCcAGAAuAAAuAUCUUcATsT 1294AD-9752 3570-3588 UCUGGGUUUUGUAGCAUUUTsT 1295 AAAUGCUACAAAACCCAGATsT1296 AD-9629 3570-3588 ucuGGGuuuuGuAGcAuuuTsT 1297AAAUGCuAcAAAACCcAGATsT 1298 AD-9755 3613-3631 AUAAAAACAAACAAACGUUTT 1299AACGUUUGUUUGUUUUUAUTT 1300 AD-15412 3617-3635 AAACAAACAAACGUUGUCCTT 1301GGACAACGUUUGUUUGUUUTT 1302 AD-15211 3618-3636 AACAAACAAACGUUGUCCUTT 1303AGGACAACGUUUGUUUGUUTT 1304 AD-15300 ¹U, C, A, G: correspondingribonucleotide; T: deoxythymidine; u, c, a, g: corresponding 2′4)-methylribonucleotide; Uf, Cf, Af, Gf: corresponding 2′-deoxy-2′-fluororibonucleotide; where nucleotides are written in sequence, they areconnected by 3′-5′ phosphodiester groups; nucleotides with interjected“s” are connected by 3′-O-5′-O phosphorothiodiester groups; unlessdenoted by prefix “p-”, oligonucleotides are devoid of a 5′-phosphategroup on the 5′-most nucleotide; all oligonucleotides bear 3′-OH on the3′-most nucleotide

TABLE 1 data IC50 in Cyno- molgous Mean percent remaining mRNAtranscript IC50 in monkey at siRNA concentration/in cell type HepG2Hepatocyte Duplex name 100 nM/HepG2 30 nM/HepG2 3 nM/HepG2 30 nM/Hela[nM] [nM]s AD-15220 35 AD-15275 56 AD-15301 70 AD-15276 42 AD-15302 32AD-15303 37 AD-15221 30 AD-15413 61 AD-15304 70 AD-15305 36 AD-15306 20AD-15307 38 AD-15277 50 AD-9526 74 89 AD-9652 97 AD-9519 78 AD-9645 66AD-9523 55 AD-9649 60 AD-9569 112 AD-9695 102 AD-15222 75 AD-15278 78AD-15178 83 AD-15308 84 AD-15223 67 AD-15309 34 AD-15279 44 AD-15194 63AD-15310 42 AD-15311 30 AD-15392 18 AD-15312 21 AD-15313 19 AD-15280 81AD-15267 82 AD-15314 32 AD-15315 74 AD-9624 94 AD-9750 96 AD-9623 43 66AD-9749 105 AD-15384 48 AD-9607 32 28 0.20 AD-9733 78 73 AD-9524 23 280.07 AD-9650 91 90 AD-9520 23 32 AD-9520 23 AD-9646 97 108 AD-9608 37AD-9734 91 AD-9546 32 AD-9672 57 AD-15385 54 AD-15393 31 AD-15316 37AD-15317 37 AD-15318 63 AD-15195 45 AD-15224 57 AD-15188 42 AD-15225 51AD-15281 89 AD-15282 75 AD-15319 61 AD-15226 56 AD-15271 25 AD-15283 25AD-15284 64 AD-15189 17 AD-15227 62 AD-9547 31 29 0.20 AD-9673 56 57AD-9548 54 60 AD-9674 36 57 AD-9529 60 AD-9655 140 AD-9605 27 31 0.27AD-9731 31 31 0.32 AD-9596 37 AD-9722 76 AD-9583 42 AD-9709 104 AD-9579113 AD-9705 81 AD-15394 32 AD-15196 72 AD-15197 85 AD-15198 71 AD-960966 71 AD-9735 115 AD-9537 145 AD-9663 102 AD-9528 113 AD-9654 107AD-9515 49 AD-9641 92 AD-9514 57 AD-9640 89 AD-9530 75 AD-9656 77AD-9538 79 80 AD-9664 53 AD-9598 69 83 AD-9724 127 AD-9625 58 88 AD-975160 AD-9556 46 AD-9682 38 AD-9539 56 63 AD-9665 83 AD-9517 36 AD-9643 40AD-9610 36 34 0.04 AD-9736 22 29 0.04 AD-14681 33 AD-14691 27 AD-1470132 AD-14711 33 AD-14721 22 AD-14731 21 AD-14741 22 AD-15087 37 AD-1509751 AD-15107 26 AD-15117 28 AD-15127 33 AD-15137 54 AD-15147 52 AD-951694 AD-9642 105 AD-9562 46 51 AD-9688 26 34 4.20 AD-14677 38 AD-14687 52AD-14697 35 AD-14707 58 AD-14717 42 AD-14727 50 AD-14737 32 AD-15083 16AD-15093 24 AD-15103 11 AD-15113 34 AD-15123 19 AD-15133 15 AD-15143 16AD-9521 50 AD-9647 62 AD-9611 48 AD-9737 68 AD-9592 46 55 AD-9718 78AD-9561 64 AD-9687 84 AD-9636 42 41 2.10 AD-9762 9 28 0.40 AD-9540 45AD-9666 81 AD-9535 48 73 AD-9661 83 AD-9559 35 AD-9685 77 AD-9533 100AD-9659 88 AD-9612 122 AD-9738 83 AD-9557 75 96 AD-9683 48 AD-9531 31 320.53 AD-9657 23 29 0.66 AD-14673 81 AD-14683 56 AD-14693 56 AD-14703 68AD-14713 55 AD-14723 24 AD-14733 34 AD-15079 85 AD-15089 54 AD-15099 70AD-15109 67 AD-15119 67 AD-15129 57 AD-15139 69 AD-9542 160 AD-9668 92AD-9739 109 AD-9637 56 83 AD-9763 79 AD-9630 82 AD-9756 63 AD-9593 55AD-9719 115 AD-9601 111 AD-9727 118 AD-9573 36 42 1.60 AD-9699 32 362.50 AD-15228 26 AD-15395 53 AD-9602 126 AD-9728 94 AD-15386 45 AD-9580112 AD-9706 86 AD-9581 35 AD-9707 81 AD-9543 51 AD-9669 97 AD-9574 74AD-9700 AD-15320 26 AD-15321 34 AD-15199 64 AD-15167 86 AD-15164 41AD-15166 43 AD-15322 64 AD-15200 46 AD-15213 27 AD-15229 44 AD-15215 49AD-15214 101 AD-9315 15 32 0.98 AD-9326 35 51 AD-9318 14 37 0.40 AD-932314 33 AD-9314 11 22 0.04 AD-10792 0.10 0.10 AD-10796 0.1 0.1 AD-9638 101AD-9764 112 AD-9525 53 AD-9651 58 AD-9560 97 AD-9686 111 AD-9536 157AD-9662 81 AD-9584 52 68 AD-9710 111 AD-15323 62 AD-9551 91 AD-9677 62AD-15230 52 AD-15231 25 AD-15285 36 AD-15396 27 AD-15397 56 AD-9600 112AD-9726 95 AD-9606 107 AD-9732 105 AD-9633 56 75 AD-9759 111 AD-9588 66AD-9714 106 AD-9589 67 85 AD-9715 113 AD-9575 120 AD-9701 100 AD-9563103 AD-9689 81 AD-9594 80 95 AD-9720 92 AD-9585 83 AD-9711 122 AD-9614100 AD-9740 198 AD-9615 116 AD-9741 130 AD-9534 32 30 AD-9534 32 AD-966089 79 AD-15324 46 AD-15232 19 AD-15233 25 AD-15234 59 AD-15286 109AD-9590 122 AD-9716 114 AD-9632 34 AD-9758 96 AD-9567 41 AD-9693 50AD-9586 81 104 AD-9712 107 AD-9564 120 AD-9690 92 AD-9616 74 84 AD-9742127 AD-15398 24 AD-9617 111 AD-9743 104 AD-9635 73 90 AD-9761 83 AD-956876 AD-9694 52 AD-9576 47 AD-9702 79 AD-9627 69 AD-9753 127 AD-9628 141AD-9754 89 AD-9631 80 AD-9757 78 AD-9595 31 32 AD-9721 87 70 AD-9544 68AD-9670 67 AD-15235 25 AD-15236 73 AD-15168 100 AD-15174 92 AD-15325 81AD-15326 65 AD-9570 35 42 AD-9696 77 AD-9566 38 AD-9692 78 AD-9532 100AD-9658 102 AD-9549 50 AD-9675 78 AD-9541 43 AD-9667 73 AD-9550 36AD-9676 100 AD-9571 27 32 AD-9697 74 89 AD-9572 47 53 AD-9698 73AD-15327 82 AD-9639 30 35 AD-9765 82 74 AD-9518 31 35 0.60 AD-9518 31AD-9644 35 37 2.60 AD-14672 26 AD-14682 27 AD-14692 22 AD-14702 19AD-14712 25 AD-14722 18 AD-14732 32 AD-15078 86 AD-15088 97 AD-15098 74AD-15108 67 AD-15118 76 AD-15128 86 AD-15138 74 AD-15237 30 AD-15287 30AD-15238 36 AD-15328 35 AD-15399 47 AD-9582 37 AD-9708 81 AD-9545 31 43AD-9671 15 33 2.50 AD-14674 16 AD-14684 26 AD-14694 18 AD-14704 27AD-14714 20 AD-14724 18 AD-14734 18 AD-15080 29 AD-15090 23 AD-15100 26AD-15110 23 AD-15120 20 AD-15130 20 AD-15140 19 AD-9522 59 AD-9648 78AD-9552 80 AD-9678 76 AD-9618 90 AD-9744 91 AD-15239 38 AD-15212 19AD-15240 43 AD-15177 59 AD-15179 13 AD-15180 15 AD-15241 14 AD-15268 42AD-15242 21 AD-15216 28 AD-15176 35 AD-15181 35 AD-15243 22 AD-15182 42AD-15244 31 AD-15387 23 AD-15245 18 AD-9555 34 AD-9681 55 AD-9619 42 61AD-9745 56 AD-9620 44 77 AD-9746 89 AD-15288 19 AD-15246 16 AD-15289 37AD-9324 59 67 AD-15329 103 AD-15330 62 AD-15169 22 AD-15201 6 AD-1533114 AD-15190 47 AD-15247 61 AD-15248 22 AD-15175 45 AD-15249 51 AD-1525096 AD-15400 12 AD-15332 22 AD-15388 30 AD-15333 20 AD-15334 96 AD-1533575 AD-15183 16 AD-15202 41 AD-15203 39 AD-15272 49 AD-15217 16 AD-1529015 AD-15218 13 AD-15389 13 AD-15336 40 AD-15337 19 AD-15191 33 AD-1539025 AD-15338 9 AD-15204 33 AD-15251 76 AD-15205 14 AD-15171 16 AD-1525258 AD-15339 20 AD-15253 15 AD-15340 18 AD-15291 17 AD-15341 11 AD-1540113 AD-15342 30 AD-15343 21 AD-15292 16 AD-15344 20 AD-15254 18 AD-1534518 AD-15206 15 AD-15346 16 AD-15347 62 AD-9577 33 31 AD-9703 17 26AD-14678 22 AD-14688 23 AD-14698 23 AD-14708 14 AD-14718 31 AD-14728 25AD-14738 31 AD-15084 19 AD-15094 11 AD-15104 16 AD-15114 15 AD-15124 11AD-15134 12 AD-15144 9 AD-15391 7 AD-15348 13 AD-15349 8 AD-15170 40AD-15350 14 AD-15402 27 AD-15293 27 AD-15351 14 AD-15403 11 AD-15404 38AD-15207 15 AD-15352 23 AD-15255 31 AD-9603 123 AD-9729 56 AD-9599 139AD-9725 38 AD-9621 77 AD-9747 63 AD-15405 32 AD-15353 39 AD-15354 49AD-15406 35 AD-15407 39 AD-15355 18 AD-15356 50 AD-15357 54 AD-15269 23AD-9565 74 AD-9691 49 AD-15358 12 AD-15359 24 AD-15360 13 AD-15219 19AD-15361 24 AD-15273 36 AD-15362 31 AD-15192 20 AD-15256 19 AD-15363 33AD-15364 24 AD-9604 35 49 AD-9730 85 AD-9527 45 AD-9653 86 AD-15365 62AD-15294 30 AD-15173 12 AD-15366 21 AD-15367 11 AD-15257 18 AD-15184 50AD-15185 12 AD-15258 73 AD-15186 36 AD-15274 19 AD-15368 7 AD-15369 17AD-15370 19 AD-15259 38 AD-15408 52 AD-9597 23 21 0.04 AD-9723 12 26AD-14680 15 AD-14690 18 AD-14700 15 AD-14710 15 AD-14720 18 AD-14730 18AD-14740 17 AD-15086 85 AD-15096 70 AD-15106 71 AD-15116 73 AD-15126 71AD-15136 56 AD-15146 72 AD-15260 79 AD-15371 24 AD-15372 52 AD-15172 27AD-15295 22 AD-15373 11 AD-15163 18 AD-15165 13 AD-15374 23 AD-15296 13AD-15261 20 AD-15375 90 AD-15262 72 AD-15376 14 AD-15377 19 AD-15409 17AD-15378 18 AD-15410 8 AD-15379 11 AD-15187 36 AD-15263 18 AD-15264 75AD-15297 21 AD-15208 6 AD-15209 28 AD-15193 131 AD-15380 88 AD-15298 43AD-15299 99 AD-15265 95 AD-15381 18 AD-15210 40 AD-15270 83 AD-9591 7595 AD-9717 105 AD-9622 94 AD-9748 103 AD-9587 63 49 AD-9713 22 25AD-14679 19 AD-14689 24 AD-14699 19 AD-14709 21 AD-14719 24 AD-14729 23AD-14739 24 AD-15085 74 AD-15095 60 AD-15105 33 AD-15115 30 AD-15125 54AD-15135 51 AD-15145 49 AD-9578 49 61 AD-9704 111 AD-9558 66 AD-9684 63AD-9634 29 30 AD-9760 14 27 AD-15411 5 AD-15266 23 AD-15382 12 AD-955423 24 AD-9680 12 22 0.10 0.10 AD-14676 12 AD-14686 13 AD-14696 12AD-14706 18 AD-14716 17 AD-14726 16 AD-14736 9 AD-15082 27 AD-15092 28AD-15102 19 AD-15112 17 AD-15122 56 AD-15132 39 AD-15142 46 AD-9553 2722 0.02 AD-9679 17 21 AD-14675 11 AD-14685 19 AD-14695 12 AD-14705 16AD-14715 19 AD-14725 19 AD-14735 19 AD-15081 30 AD-15091 16 AD-15101 16AD-15111 11 AD-15121 19 AD-15131 17 AD-15141 18 AD-9626 97 68 AD-9752 2833 AD-9629 23 24 AD-9755 28 29 AD-15412 21 AD-15211 73 AD-15300 41

TABLE 2 SEQ SEQ Duplex ID ID number Sense strand sequence (5′-3′)¹ NO:Antisense-strand sequence (5′-3′)¹ NO: AD-10792 GccuGGAGuuuAuucGGAATsT1305 UUCCGAAuAAACUCcAGGCTsT 1306 AD-10793 GccuGGAGuuuAuucGGAATsT 1307uUcCGAAuAAACUccAGGCTsT 1308 AD-10796 GccuGGAGuuuAuucGGAATsT 1309UUCCGAAUAAACUCCAGGCTsT 1310 AD-12038 GccuGGAGuuuAuucGGAATsT 1311uUCCGAAUAAACUCCAGGCTsT 1312 AD-12039 GccuGGAGuuuAuucGGAATsT 1313UuCCGAAUAAACUCCAGGCTsT 1314 AD-12040 GccuGGAGuuuAuucGGAATsT 1315UUcCGAAUAAACUCCAGGCTsT 1316 AD-12041 GccuGGAGuuuAuucGGAATsT 1317UUCcGAAUAAACUCCAGGCTsT 1318 AD-12042 GCCUGGAGUUUAUUCGGAATsT 1319uUCCGAAUAAACUCCAGGCTsT 1320 AD-12043 GCCUGGAGUUUAUUCGGAATsT 1321UuCCGAAUAAACUCCAGGCTsT 1322 AD-12044 GCCUGGAGUUUAUUCGGAATsT 1323UUcCGAAUAAACUCCAGGCTsT 1324 AD-12045 GCCUGGAGUUUAUUCGGAATsT 1325UUCcGAAUAAACUCCAGGCTsT 1326 AD-12046 GccuGGAGuuuAuucGGAA 1327UUCCGAAUAAACUCCAGGCscsu 1328 AD-12047 GccuGGAGuuuAuucGGAAA 1329UUUCCGAAUAAACUCCAGGCscsu 1330 AD-12048 GccuGGAGuuuAuucGGAAAA 1331UUUUCCGAAUAAACUCCAGGCscsu 1332 AD-12049 GccuGGAGuuuAuucGGAAAAG 1333CUUUUCCGAAUAAACUCCAGGCscsu 1334 AD-12050 GccuGGAGuuuAuucGGAATTab 1335UUCCGAAUAAACUCCAGGCTTab 1336 AD-12051 GccuGGAGuuuAuucGGAAATTab 1337UUUCCGAAuAAACUCCAGGCTTab 1338 AD-12052 GccuGGAGuuuAuucGGAAAATTab 1339UUUUCCGAAUAAACUCCAGGCTTab 1340 AD-12053 GccuGGAGuuuAuucGGAAAAGTTab 1341CUUUUCCGAAUAAACUCCAGGCTTab 1342 AD-12054 GCCUGGAGUUUAUUCGGAATsT 1343UUCCGAAUAAACUCCAGGCscsu 1344 AD-12055 GccuGGAGuuuAuucGGAATsT 1345UUCCGAAUAAACUCCAGGCscsu 1346 AD-12056 GcCuGgAgUuUaUuCgGaA 1347UUCCGAAUAAACUCCAGGCTTab 1348 AD-12057 GcCuGgAgUuUaUuCgGaA 1349UUCCGAAUAAACUCCAGGCTsT 1350 AD-12058 GcCuGgAgUuUaUuCgGaA 1351UUCCGAAuAAACUCcAGGCTsT 1352 AD-12059 GcCuGgAgUuUaUuCgGaA 1353uUcCGAAuAAACUccAGGCTsT 1354 AD-12060 GcCuGgAgUuUaUuCgGaA 1355UUCCGaaUAaaCUCCAggc 1356 AD-12061 GcCuGgnAgUuUaUuCgGaATsT 1357UUCCGaaUAaaCUCCAggcTsT 1358 AD-12062 GcCuGgAgUuUaUuCgGaATTab 1359UUCCGaaUAaaCUCCAggcTTab 1360 AD-12063 GcCuGgAgUuUaUuCgGaA 1361UUCCGaaUAaaCUCCAggcscsu 1362 AD-12064 GcCuGgnAgUuUaUuCgGaATsT 1363UUCCGAAuAAACUCcAGGCTsT 1364 AD-12065 GcCuGgAgUuUaUuCgGaATTab 1365UUCCGAAuAAACUCcAGGCTTab 1366 AD-12066 GcCuGgAgUuUaUuCgGaA 1367UUCCGAAuAAACUCcAGGCscsu 1368 AD-12067 GcCuGgnAgUuUaUuCgGaATsT 1369UUCCGAAUAAACUCCAGGCTsT 1370 AD-12068 GcCuGgAgUuUaUuCgGaATTab 1371UUCCGAAUAAACUCCAGGCTTab 1372 AD-12069 GcCuGgAgUuUaUuCgGaA 1373UUCCGAAUAAACUCCAGGCscsu 1374 AD-12338 GfcCfuGfgAfgUfuUfaUfuCfgGfaAf 1375P-uUfcCfgAfaUfaAfaCfuCfcAfgGfc 1376 AD-12339 GcCuGgAgUuUaUuCgGaA 1377P-uUfcCfgAfaUfaAfaCfuCfcAfgGfc 1378 AD-12340 GccuGGAGuuuAuucGGAA 1379P-uUfcCfgAfaUfaAfaCfuCfcAfgGfc 1380 AD-12341GfcCfuGfgAfgUfuUfaUfuCfgGfaAfTsT 1381 P-uUfcCfgAfaUfaAfaCfuCfcAfgGfcTsT1382 AD-12342 GfcCfuGfgAfgUfuUfaUfuCfgGfaAfTsT 1383UUCCGAAuAAACUCcAGGCTsT 1384 AD-12343 GfcCfuGfgAfgUfuUfaUfuCfgGfaAfTsT1385 uUcCGAAuAAACUccAGGCTsT 1386 AD-12344GfcCfuGfgAfgUfuUfaUfuCfgGfaAfTsT 1387 UUCCGAAUAAACUCCAGGCTsT 1388AD-12345 GfcCfuGfgAfgUfuUfaUfuCfgGfaAfTsT 1389 UUCCGAAUAAACUCCAGGCscsu1390 AD-12346 GfcCfuGfgAfgUfuUfaUfuCfgGfaAfTsT 1391UUCCGaaUAaaCUCCAggcscsu 1392 AD-12347 GCCUGGAGUUUAUUCGGAATsT 1393P-uUfcCfgAfaUfaAfaCfuCfcAfgGfcTsT 1394 AD-12348 GccuGGAGuuuAuucGGAATsT1395 P-uUfcCfgAfaUfaAfaCfuCfcAfgGfcTsT 1396 AD-12349GcCuGgnAgUuUaUuCgGaATsT 1397 P-uUfcCfgAfaUfaAfaCfuCfcAfgGfcTsT 1398AD-12350 GfcCfuGfgAfgUfuUfaUfuCfgGfaAfTTab 1399P-uUfcCfgAfaUfaAfaCfuCfcAfgGfcTTab 1400 AD-12351GfcCfuGfgAfgUfuUfaUfuCfgGfaAf 1401 P-uUfcCfgAfaUfaAfaCfuCfcAfgGfcsCfsu1402 AD-12352 GfcCfuGfgAfgUfuUfaUfuCfgGfaAf 1403 UUCCGaaUAaaCUCCAggcscsu1404 AD-12354 GfcCfuGfgAfgUfuUfaUfuCfgGfaAf 1405 UUCCGAAUAAACUCCAGGCscsu1406 AD-12355 GfcCfuGfgAfgUfuUfaUfuCfgGfaAf 1407 UUCCGAAuAAACUCcAGGCTsT1408 AD-12356 GfcCfuGfgAfgUfuUfaUfuCfgGfaAf 1409 uUcCGAAuAAACUccAGGCTsT1410 AD-12357 GmocCmouGmogAm02gUmouUmoaUmouC 1411 UUCCGaaUAaaCUCCAggc1412 mogGmoaA AD-12358 GmocCmouGmogAm02gUmouUmoaUmouC 1413P-uUfcCfgAfaUfaAfaCfuCfcAfgGfc 1414 mogGmoaA AD-12359GmocCmouGmogAm02gUmouUmoaUmouC 1415 P-uUfcCfgAfaUfaAfaCfuCfcAfgGfcsCfsu1416 mogGmoaA AD-12360 GmocCmouGmogAm02gUmouUmoaUmouC 1417UUCCGAAUAAACUCCAGGCscsu 1418 mogGmoaA AD-12361GmocCmouGmogAm02gUmouUmoaUmouC 1419 UUCCGAAuAAACUCcAGGCTsT 1420 mogGmoaAAD-12362 GmocCmouGmogAm02gUmouUmoaUmouC 1421 uUcCGAAuAAACUccAGGCTsT 1422mogGmoaA AD-12363 GmocCmouGmogAm02gUmouUmoaUmouC 1423UUCCGaaUAaaCUCCAggcscsu 1424 mogGmoaA AD-12364GmocCmouGmogAmogUmouUmoaUmouCm 1425 UUCCGaaUAaaCUCCAggcTsT 1426ogGmoaATsT AD-12365 GmocCmouGmogAmogUmouUmoaUmouCm 1427UUCCGAAuAAACUCcAGGCTsT 1428 ogGmoaATsT AD-12366GmocCmouGmogAmogUmouUmoaUmouCm 1429 UUCCGAAUAAACUCCAGGCTsT 1430ogGmoaATsT AD-12367 GmocmocmouGGAGmoumoumouAmoumou 1431UUCCGaaUAaaCUCCAggcTsT 1432 mocGGAATsT AD-12368GmocmocmouGGAGmoumoumouAmoumou 1433 UUCCGAAuAAACUCcAGGCTsT 1434mocGGAATsT AD-12369 GmocmocmouGGAGmoumoumouAmoumou 1435UUCCGAAUAAACUCCAGGCTsT 1436 mocGGAATsT AD-12370GmocmocmouGGAGmoumoumouAmoumou 1437 P-UfaCfCfGAAUfAAACMCfCfAGGCfTsT 1438mocGGAATsT AD-12371 GmocmocmouGGAGmoumoumouAmoumou 1439P-UfUfCfCfGAAUfAAACfUfCfCfAGGCfsCfsUf 1440 mocGGAATsT AD-12372GmocmocmouGGAGmoumoumouAmoumou 1441 P-uUfcCfgAfaUfaAfaCfuCfcAfgGfcsCfsu1442 mocGGAATsT AD-12373 GmocmocmouGGAGmoumoumouAmoumou 1443UUCCGAAUAAACUCCAGGCTsT 1444 mocGGAATsT AD-12374GCfCfUfGGAGUfUfUfAUfUfCfGGAATsT 1445 UfUfCfCfGAAUfAAACfUfCfCfAGGCfTsT1446 AD-12375 GCfCfUfGGAGUfUfUfAUfUfCfGGAATsT 1447UUCCGAAUAAACUCCAGGCTsT 1448 AD-12377 GCfCfUfGGAGUfUfUfAUfUfCfGGAATsT1449 uUcCGAAuAAACUccAGGCTsT 1450 AD-12378GCfCfUfGGAGUfUfUfAUfUfCfGGAATsT 1451 UUCCGaaUAaaCUCCAggcscsu 1452AD-12379 GCfCfUfGGAGUfUfUfAUfUfCfGGAATsT 1453 UUCCGAAUAAACUCCAGGCscsu1454 AD-12380 GCfCfUfGGAGUfUfUfAUfUfCfGGAATsT 1455P-uUfcCfgAfaUfaAfaCfuCfcAfgGfcsCfsu 1456 AD-12381GCfCfUfGGAGUfUfUfAUfUfCfGGAATsT 1457 P-uUfc CfgAfaUfaAfaCfuCfcAfgGfcTsT1458 AD-12382 GCfCfUfGGAGUfUfUfAUfUfCfGGAATsT 1459P-UfUfCfCfGAAUfAAACfUfCfCfAGGCfTsT 1460 AD-12383 GCCUGGAGUUUAUUCGGAATsT1461 P-UfUfCfCfGAAUfAAACfUfCfCfAGGCfTsT 1462 AD-12384GccuGGAGuuuAuucGGAATsT 1463 P-UfUfCfCfGAAUfAAACfUfCfCfAGGCfTsT 1464AD-12385 Gc Cu GgnAgUuUaUuCg GaATsT 1465P-UfUfCfCfGAAUfAAACfUfCfCfAGGCfTsT 1466 AD-12386GfcCfuGfgAfgUfuUfaUfuCfgGfaAf 1467 P-UfUfCfCfGAAUfAAACfUfCfCfAGGCfTsT1468 AD-12387 GCfCfUfGGAGGUfUfUfAUfUfCfGGAA 1469UfUfCfCfGAAUfAAACfUfCfCfAGGCfsCfsUf 1470 AD-12388GCfCfUfGGAGGUfUfUfAUfUfCfGGAA 1471 P-uUfcCfgAfaUfaAfaCfuCfcAfgGfc 1472AD-12389 GCfCfUfGGAGGUfUfUfAUfUfCfGGAA 1473P-uUfcCfgAfaUfaAfaCfuCfcAfgGfcsCfsu 1474 AD-12390GCfCfUfGGAGGUfUfUfAUfUfCfGGAA 1475 UUCCGAAUAAACUCCAGGCscsu 1476 AD-12391GCfCfUfGGAGGUfUfUfAUfUfCfGGAA 1477 UUCCGaaUAaaCUCCAggc 1478 AD-12392GCfCfUfGGAGGUfUfUfAUfUfCfGGAA 1479 UUCCGAAUAAACUCCAGGCTsT 1480 AD-12393GCfCfUfGGAGGUfUfUfAUfUfCfGGAA 1481 UUCCGAAuAAACUCcAGGCTsT 1482 AD-12394GCfCfUfGGAGGUfUfUfAUfUfCfGGAA 1483 uUcCGAAuAAACUccAGGCTsT 1484 AD-12395GmocCmouGmogAmogUmouUmoaUmouCm 1485 P-UfUfCfCfGAAUfAAACfUfCfCfAGGCfsCf1486 ogGmoaATsT sUf AD-12396 GmocCmouGmogAm02gUmouUmoaUmouC 1487P-UfUfCfCfGAAUfAAACfUfCfCfAGGCfsCf 1488 mogGmoaA sUf AD-12397GfcCfuGfgAfgUfuUfaUfuCfgGfaAf 1489 P-UfUfCfCfGAAUfAAACfUfCfCfAGGCfsCf1490 sUf AD-12398 GfcCfuGfgAfgUfuUfaUfuCfgGfaAfTsT 1491P-UfUfCfCfGAAUfAAACfUfCfCfAGGCfsCf 1492 sUf AD-12399GcCuGgnAgUuUaUuCgGaATsT 1493 P-UfUfCfCfGAAUfAAACfUfCfCfAGGCfsCf 1494 sUfAD-12400 GCCUGGAGUUUAUUCGGAATsT 1495 P-UfUfCfCfGAAUfAAACfUfCfCfAGGCfsCf1496 sUf AD-12401 GccuGGAGuuuAuucGGAATsT 1497P-UfUfCfCfGAAUfAAACfUfCfCfAGGCfsCf 1498 sUf AD-12402 GccuGGAGuuuAuucGGAA1499 P-UfUfCfCfGAAUfAAACfUfCfCfAGGCfsCf 1500 sUf AD-12403GCfCfUfGGAGGUfUfUfAUfUfCfGGAA 1501 P-UfUfCfCfGAAUfAAACfUfCfCfAGGCfsCf1502 sUf AD-9314 GCCUGGAGUUUAUUCGGAATsT 1503 UUCCGAAUAAACUCCAGGCTsT 1504¹U, C, A, G: corresponding ribonucleotide; T: deoxythymidine; u, c, a,g: corresponding 2′-O-methyl ribonucleotide; Uf, Cf, Af, Gf:corresponding 2′-deoxy-2′-fluoro ribonucleotide; moc, mou, mog, moa:corresponding 2′-MOE nucleotide; where nucleotides are written insequence, they are connected by 3′-5′ phosphodiester groups; ab:3′-terminal abasic nucleotide; nucleotides with interjected “s” areconnected by 3′-O-5′-O phosphorothiodiester groups; unless denoted byprefix “p-”, oligonucleotides are devoid of a 5′-phosphate group on the5′-most 3′-OH on the 3′-most nucleotide nucleotide; all oligonucleotidesbear

TABLE 2 Remaining mRNA in % of controls at Duplex number siRNA conc. of30 nM AD-10792 15 AD-10793 32 AD-10796 13 AD-12038 13 AD-12039 29AD-12040 10 AD-12041 11 AD-12042 12 AD-12043 13 AD-12044 7 AD-12045 8AD-12046 13 AD-12047 17 AD-12048 43 AD-12049 34 AD-12050 16 AD-12051 31AD-12052 81 AD-12053 46 AD-12054 8 AD-12055 13 AD-12056 11 AD-12057 8AD-12058 9 AD-12059 23 AD-12060 10 AD-12061 7 AD-12062 10 AD-12063 19AD-12064 15 AD-12065 16 AD-12066 20 AD-12067 17 AD-12068 18 AD-12069 13AD-12338 15 AD-12339 14 AD-12340 19 AD-12341 12 AD-12342 13 AD-12343 24AD-12344 9 AD-12345 12 AD-12346 13 AD-12347 11 AD-12348 8 AD-12349 11AD-12350 17 AD-12351 11 AD-12352 11 AD-12354 11 AD-12355 9 AD-12356 25AD-12357 56 AD-12358 29 AD-12359 30 AD-12360 15 AD-12361 20 AD-12362 51AD-12363 11 AD-12364 25 AD-12365 18 AD-12366 23 AD-12367 42 AD-12368 40AD-12369 26 AD-12370 68 AD-12371 60 AD-12372 60 AD-12373 55 AD-12374 9AD-12375 16 AD-12377 88 AD-12378 6 AD-12379 6 AD-12380 8 AD-12381 10AD-12382 7 AD-12383 7 AD-12377 88 AD-12378 6 AD-12379 6 AD-12380 8AD-12381 10 AD-12382 7 AD-12383 7 AD-12384 8 AD-12385 8 AD-12386 11AD-12387 13 AD-12388 19 AD-12389 16 AD-12390 17 AD-12391 21 AD-12392 28AD-12393 17 AD-12394 75 AD-12395 55 AD-12396 59 AD-12397 20 AD-12398 11AD-12399 13 AD-12400 12 AD-12401 13 AD-12402 14 AD-12403 4 AD-9314 9

1. A double-stranded ribonucleic acid (dsRNA) for inhibiting expressionof a human proprotein convertase subtilisin kexin 9 (PCSK9) gene in acell, wherein the dsRNA comprises a sense strand and an antisense strandcomplementary to at least 15 contiguous nucleotides of a PCSK9 gene andcomprises a duplex structure between 15 and 30 base pairs in length. 2.The dsRNA of claim 1 comprising a duplex structure between 19 and 21base pairs in length.
 3. The dsRNA of claim 1 wherein the sense strandcomprises the nucleotide sequence of of a sense strand of Table 1 andthe antisense strand comprises the nucleotide sequence of an antisensestrand of Table
 1. 4. The dsRNA of claim 1, consisting of a sense strandand an antisense strand of Table
 1. 5. The dsRNA of claim 1, consistingof a modified dsRNA of Table
 2. 6. The dsRNA of claim 1, wherein thedsRNA comprises at least one modified nucleotide.
 7. The dsRNA of claim1, wherein the dsRNA comprises at least one 2′-O-methyl modifiednucleotide and at least one nucleotide comprising a 5′-phosphorothioategroup.
 8. The dsRNA claim 1, wherein the dsRNA comprises at least onemodified nucleotide, wherein the modified nucleotide is chosen from thegroup of: a 2′-O-methyl modified nucleotide, a 2′-deoxy-2′-fluoromodified nucleotide, a 2′-deoxy-modified nucleotide, a lockednucleotide, an abasic nucleotide, 2′-amino-modified nucleotide,2′-alkyl-modified nucleotide, a morpholino nucleotide, aphosphoramidate, a nucleotide comprising a 5′-phosphorothioate group, aterminal nucleotide linked to a cholesteryl derivative or dodecanoicacid bisdecylamide group, and a non-natural base comprising nucleotide.9. A cell comprising the dsRNA of claim
 1. 10. A pharmaceuticalcomposition comprising the dsRNA of claim 1 and a pharmaceuticallyacceptable carrier.
 11. A composition comprising the dsRNA of claim 1and a lipid formulation.
 12. A composition comprising the dsRNA of claim1 and a lipid formulation, wherein the lipid formulation comprises acationic lipid comprising ND-98.
 13. A vector comprising a regulatorysequence operably linked to a nucleotide sequence that encodes at leastone strand of the dsRNA of claim
 1. 14. A cell comprising the vector ofclaim
 13. 15. The dsRNA of claim 1, wherein contacting a cell in vitrowith 30 nM or less of the dsRNA and maintaining the cell for a timesufficient to obtain degradation of a mRNA transcript of a PCSK9 gene,inhibits expression of the PCSK9 gene in the cell.
 16. The dsRNA ofclaim 1, wherein contacting HepG2 cells expressing the PCSK9 gene invitro with the dsRNA and maintaining the cells for a time sufficient toobtain degradation of a mRNA transcript of a PCSK9 gene, inhibitsexpression of the PCSK9 gene in the cell by at least 20%.
 17. The dsRNAof claim 1, wherein administering the dsRNA to an animal decreases totalserum cholesterol in the animal.
 18. A method for inhibiting expressionof a proprotein convertase subtilisin kexin 9 (PCSK9) gene in a cellcomprising contacting the cell with the dsRNAof claim 1 and maintainingthe cell for a time sufficient to obtain degradation of a mRNAtranscript of a PCSK9 gene, thereby inhibiting expression of the PCSK9gene in the cell.
 19. A method of treating or managing pathologicalprocesses which can be mediated by down regulating expression of aproprotein convertase subtilisin kexin 9 (PCSK9) gene comprisingadministering to a patient in need of such treatment or management atherapeutically effective amount of the dsRNA of claim 1.